{"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578729;vdb=variation;vf=341147089\">rs543578729</a>","highlight":"","entries":[{"key":"Class","value":"SNP"},{"value":"dbSNP","key":"Source"},{"value":"5:40846482","key":"Location"},{"key":"Alleles","value":"C/G/T (Forward strand)"},{"key":"Consequences","value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#02599c\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant occurring within an intron\">intron variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#a52a2a\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant located within a regulatory region\">regulatory region variant</span></nobr><li></ul>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578729;vdb=variation;vf=341147089\">Explore this variant</a>"},{"value":"<a href=\"/Homo_sapiens/Variation/Mappings?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578729;vdb=variation;vf=341147089\">Gene/Transcript Locations</a>","key":null},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Population?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578729;vdb=variation;vf=341147089\">Population Allele Frequencies</a>","class":"population"},{"key":"ALL","childOf":"population","value":"<span class=\"freq base_T\" style=\"width:0px\"></span><span class=\"freq base_C\" style=\"width:100px\"></span><div>T: 0.000, C: 1.000</div>"},{"value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>","childOf":"population","key":"AFR"},{"key":"AMR","value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>","childOf":"population"},{"key":"EAS","childOf":"population","value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>"},{"key":"EUR","value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>","childOf":"population"},{"value":"<span class=\"freq base_T\" style=\"width:0.1px\"></span><span class=\"freq base_C\" style=\"width:99.9px\"></span><div>T: 0.001, C: 0.999</div>","childOf":"population","key":"SAS"}]},{"highlight":"","caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578694;vdb=variation;vf=341147088\">rs543578694</a>","entries":[{"key":"Class","value":"SNP"},{"value":"dbSNP","key":"Source"},{"value":"5:46022794","key":"Location"},{"key":"Alleles","value":"T/C (Forward strand)"},{"value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#636363\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant located in the intergenic region, between genes\">intergenic variant</span></nobr><li></ul>","key":"Consequences"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578694;vdb=variation;vf=341147088\">Explore this variant</a>"},{"key":null,"class":"population","value":"<a href=\"/Homo_sapiens/Variation/Population?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578694;vdb=variation;vf=341147088\">Population Allele Frequencies</a>"},{"childOf":"population","value":"<span class=\"freq base_T\" style=\"width:100px\"></span><span class=\"freq base_C\" style=\"width:0px\"></span><div>T: 1.000, C: 0.000</div>","key":"ALL"},{"value":"<span class=\"freq base_T\" style=\"width:99.9px\"></span><span class=\"freq base_C\" style=\"width:0.1px\"></span><div>T: 0.999, C: 0.001</div>","childOf":"population","key":"AFR"},{"key":"AMR","childOf":"population","value":"<span class=\"freq base_T\" style=\"width:100px\"></span><div>T: 1.000</div>"},{"key":"EAS","childOf":"population","value":"<span class=\"freq base_T\" style=\"width:100px\"></span><div>T: 1.000</div>"},{"childOf":"population","value":"<span class=\"freq base_T\" style=\"width:100px\"></span><div>T: 1.000</div>","key":"EUR"},{"key":"SAS","childOf":"population","value":"<span class=\"freq base_T\" style=\"width:100px\"></span><div>T: 1.000</div>"}]},{"entries":[{"value":"SNP","key":"Class"},{"key":"Source","value":"dbSNP"},{"key":"Location","value":"5:121317286"},{"value":"G/A (Forward strand)","key":"Alleles"},{"value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#02599c\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant occurring within an intron\">intron variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#32cd32\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant of a non coding RNA gene\">non coding transcript variant</span></nobr><li></ul>","key":"Consequences"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578732;vdb=variation;vf=341147090\">Explore this variant</a>","key":null},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Population?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578732;vdb=variation;vf=341147090\">Population Allele Frequencies</a>","class":"population"},{"key":"ALL","value":"<span class=\"freq base_A\" style=\"width:0px\"></span><span class=\"freq base_G\" style=\"width:100px\"></span><div>A: 0.000, G: 1.000</div>","childOf":"population"},{"value":"<span class=\"freq base_G\" style=\"width:99.9px\"></span><span class=\"freq base_A\" style=\"width:0.1px\"></span><div>G: 0.999, A: 0.001</div>","childOf":"population","key":"AFR"},{"childOf":"population","value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>","key":"AMR"},{"value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>","childOf":"population","key":"EAS"},{"value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>","childOf":"population","key":"EUR"},{"value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>","childOf":"population","key":"SAS"}],"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578732;vdb=variation;vf=341147090\">rs543578732</a>","highlight":""}],"header":null}