| Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
|---|---|---|---|---|---|
| chr13 | 110948985 | 110956594 | enh15495 |
|
|
| chr13 | 110950675 | 110951614 | vista17035 |
|
| Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
|---|---|---|---|---|---|---|---|---|
| chr13 | 110951091 | 110951620 | TCF7L2 | GTRD | no | Colon (HCT116) | 108089140 | |
| chr13 | 110951109 | 110951747 | TCF7L2 | GTRD | no | Colon (HCT116) | 108089141 | |
| chr13 | 110951222 | 110951671 | TCF7L2 | GTRD | no | Colon (HCT116) | 108089142 | |
| chr13 | 110951395 | 110951915 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 108089143 |
| Chrom. | Start | End | Strand | Gene name | Ensembl ID | TSS of gene | Distance between TSS and SNP | Tissue | q Value | id | More |
|---|