| Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
|---|
| Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
|---|---|---|---|---|---|---|---|---|
| chr16 | 11489403 | 11490529 | TCF7L2 | GTRD | no | Colon (HCT116) | 108181751 | |
| chr16 | 11489411 | 11490552 | TCF7L2 | GTRD | no | Colon (HCT116) | 108181752 | |
| chr16 | 11489636 | 11490429 | ZNF274 | GTRD | no | Liver (HepG2) | 108181760 | |
| chr16 | 11489788 | 11490435 | ZNF274 | GTRD | no | Liver (HepG2) | 108181765 | |
| chr16 | 11489925 | 11490416 | ZNF274 | GTRD | no | Liver (HepG2) | 108181767 | |
| chr16 | 11490036 | 11490500 | ZZZ3 | ENCODE Uniform TFBS | no | Cervix (HeLa-S3) | 108181768 | |
| chr16 | 11490040 | 11490560 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 108181769 | |
| chr16 | 11490054 | 11490669 | CTCF | UCSC Txn Factor | no | Conserved | 108181770 |
| Chrom. | Start | End | Strand | Gene name | Ensembl ID | TSS of gene | Distance between TSS and SNP | Tissue | q Value | id | More |
|---|