EnhancerDB
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  3. rs564390568[chr14:104007192]
Enhancers that have rs564390568[chr14:104007192]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 104001265 104021295 enh15979
Brain (SK-N-MC) Astrocyte Colon (HCT116) Embryonic Stem Cell Line (H1-hESC) Uterus Stomach Brain (SK-N-SH) Bone (Osteoblast) Thyroid Pancreas (Panc1) Prostate (PC-3) Cervix (HeLa-S3) Esophagus Placenta Lung (PC-9) Muscle (Myoblast) Breast Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Muscle (A673) Heart
Transcript factors that have rs564390568[chr14:104007192]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 104006571 104007231 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643991
chr14 104006718 104007222 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643992
chr14 104006856 104007260 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643993
chr14 104006865 104007261 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643994
chr14 104006892 104007212 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643995
chr14 104006989 104007505 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643997
chr14 104007096 104007626 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643998
chr14 104007150 104007495 TCF7L2 GTRD no Colon (HCT116) 21643999
chr14 104007190 104007205 STAT2 JASPAR yes 117993692
Genes associated with rs564390568[chr14:104007192], 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