| Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
|---|---|---|---|---|---|
| chr11 | 1089762 | 1090061 | vista9328 |
|
| Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
|---|---|---|---|---|---|---|---|---|
| chr11 | 1088690 | 1090832 | TCF7L2 | GTRD | no | Colon (HCT116) | 107950851 | |
| chr11 | 1088989 | 1089882 | TCF7L2 | GTRD | no | Colon (HCT116) | 107950852 | |
| chr11 | 1089431 | 1090470 | TCF7L2 | GTRD | no | Colon (HCT116) | 107950853 | |
| chr11 | 1089603 | 1089913 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 107950854 | |
| chr11 | 1089788 | 1089803 | TP53 | JASPAR | yes | 114026950 |
| Chrom. | Start | End | Strand | Gene name | Ensembl ID | TSS of gene | Distance between TSS and SNP | Tissue | q Value | id | More |
|---|