Enhancers that have rs12886191[chr14:105191400]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 105191285 105191466 vista19247

Transcript factors that have rs12886191[chr14:105191400]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 105190568 105191923 TCF7L2 GTRD no Colon (HCT116) 108127788
chr14 105190589 105192106 TCF7L2 GTRD no Colon (HCT116) 108127790
chr14 105190611 105192320 ZNF143 GTRD no Epithelial (MCF-7) 108127791
chr14 105190635 105192228 ZNF143 GTRD no Epithelial (MCF-7) 108127792
chr14 105190642 105192225 ZNF143 GTRD no Epithelial (MCF-7) 108127793
chr14 105191032 105191692 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108127798
chr14 105191136 105191786 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108127799
chr14 105191140 105191510 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108127800
chr14 105191301 105191677 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108127801
chr14 105191343 105191752 TCF7L2 GTRD no Colon (HCT116) 108127802
chr14 105191343 105192196 TCF7L2 GTRD no Colon (HCT116) 108127803
chr14 105191347 105191753 CTCF UCSC Txn Factor no Conserved 108127804
chr14 105191385 105191961 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 108127805
chr14 105191393 105191855 ZNF274 GTRD no Bone Marrow (K562) 108127806

Genes associated with rs12886191[chr14:105191400], 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