EnhancerDB
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  3. rs140646227[chr14:57322756]
Enhancers that have rs140646227[chr14:57322756]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 57319145 57327435 enh51834
Stomach Large Intestine Embryonic Stem Cell Line (H1-hESC)
chr14 57320664 57324319 vista463
VISTA
Transcript factors that have rs140646227[chr14:57322756]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 57322482 57323152 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21620865
chr14 57322600 57323120 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21620866
chr14 57322609 57322865 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21620867
chr14 57322613 57323223 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21620868
chr14 57322625 57322949 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21620869
chr14 57322671 57322995 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21620870
chr14 57322714 57323038 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21620871
Genes associated with rs140646227[chr14:57322756], 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