EnhancerDB
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  3. rs34864500[chr14:102977216]
Enhancers that have rs34864500[chr14:102977216]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 102977207 102977381 vista19170
VISTA
Transcript factors that have rs34864500[chr14:102977216]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 102976404 102977409 TCF7L2 GTRD no Colon (HCT116) 108125818
chr14 102977024 102977384 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 108125819
chr14 102977066 102977390 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108125820
chr14 102977068 102977318 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108125821
chr14 102977126 102977516 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 108125822
chr14 102977131 102977335 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 108125823
chr14 102977147 102977771 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 108125824
chr14 102977175 102977575 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 108125825
chr14 102977179 102977555 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108125826
chr14 102977186 102977606 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 108125827
chr14 102977194 102977554 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 108125828
chr14 102977212 102977216 NFE TRANSFAC yes 107614840
Genes associated with rs34864500[chr14:102977216], 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