Enhancers that have rs114625401[chr16:1047072]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 1045545 1050015 enh88212

Transcript factors that have rs114625401[chr16:1047072]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 1043552 1049740 TCF7L2 GTRD no Colon (HCT116) 108170980
chr16 1043582 1047178 TCF7L2 GTRD no Colon (HCT116) 108170981
chr16 1043594 1047476 TCF7L2 GTRD no Colon (HCT116) 108170982
chr16 1043614 1047490 TCF7L2 GTRD no Colon (HCT116) 108170983
chr16 1043655 1047419 TCF7L2 GTRD no Colon (HCT116) 108170984
chr16 1046067 1047215 ZNF143 GTRD no Epithelial (MCF-7) 108170986
chr16 1046467 1047532 TCF7L2 GTRD no Colon (HCT116) 108170987
chr16 1046626 1047182 TCF7L2 GTRD no Colon (HCT116) 108170988
chr16 1046855 1050010 ZNF143 GTRD no Epithelial (MCF-7) 108170989
chr16 1046880 1047440 ZNF274 GTRD no Bone Marrow (K562) 108170990
chr16 1046881 1047111 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21684042
chr16 1046881 1047111 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108170991
chr16 1047052 1047073 ZNF263 JASPAR yes 9128557
chr16 1047066 1047076 SP1 JASPAR yes 9128561
chr16 1047072 1047077 SP1 TRANSFAC yes 9128562

Genes associated with rs114625401[chr16:1047072], 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
chr16 226679 227521 + HBA1 ENSG00000206172.4 226679 819551 Esophagus 0.0456953 14334
chr16 731671 734529 - JMJD8 ENSG00000161999.7 734529 312543 Uterus 0.451775 14360