Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
---|
Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
---|---|---|---|---|---|---|---|---|
chr19 | 1750357 | 1760948 | TCF7L2 | GTRD | no | Colon (HCT116) | 21832612 | |
chr19 | 1750357 | 1760948 | TCF7L2 | GTRD | no | Colon (HCT116) | 108355142 | |
chr19 | 1751288 | 1756772 | TCF7L2 | GTRD | no | Colon (HCT116) | 108355143 | |
chr19 | 1751968 | 1756658 | TCF7L2 | GTRD | no | Colon (HCT116) | 108355144 | |
chr19 | 1754463 | 1758835 | EZH2 | UCSC Txn Factor | no | Conserved | 108355147 | |
chr19 | 1754491 | 1756662 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 108355148 |
Chrom. | Start | End | Strand | Gene name | Ensembl ID | TSS of gene | Distance between TSS and SNP | Tissue | q Value | id | More |
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