EnhancerDB
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  3. rs569261282[chr14:99712138]
Enhancers that have rs569261282[chr14:99712138]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 99711955 99712816 vista19037
VISTA
Transcript factors that have rs569261282[chr14:99712138]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 99711842 99712322 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21637802
chr14 99711842 99712322 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108122071
chr14 99711932 99712268 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21637803
chr14 99711932 99712268 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108122072
chr14 99712123 99712793 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108122073
Genes associated with rs569261282[chr14:99712138], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom. Start End Strand Gene name Ensembl ID TSS of gene Distance between TSS and SNP Tissue q Value id More