EnhancerDB
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  3. rs397721336[chr14:103660652]
Enhancers that have rs397721336[chr14:103660652]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 103649674 103677715 enh15975
Bone Marrow (K562) Liver (HepG2) Cervix (HeLa-S3) Brain (SK-N-MC) Large Intestine Prostate (RWPE1) Esophagus Astrocyte Bone (Osteoblast) Stomach Placenta Uterus Embryonic Stem Cell Line (H1-hESC) Lung (PC-9) Pancreas Pancreas (Panc1) Neural Stem Cells (H9) Epithelial (MCF-7)
Transcript factors that have rs397721336[chr14:103660652]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 103660603 103660923 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643332
chr14 103660612 103661008 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643333
chr14 103660615 103660955 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643334
chr14 103660632 103660956 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 21643335
chr14 103660637 103660981 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643336
chr14 103660641 103660961 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643337
chr14 103660645 103660975 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643338
chr14 103660651 103660657 TBP TRANSFAC yes 117965914
Genes associated with rs397721336[chr14:103660652], 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