| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:11841839-11842079 | Common:3; Rare:79 | ||||
| chr11:12377472-12377643 | Rare:70 | ||||
| chr11:13463151-13463336 | Common:1; Rare:67 | ||||
| chr11:14499782-14499976 | Common:3; Rare:59 | ||||
| chr11:14520314-14520558 | Rare:79 | ||||
| chr11:14643631-14643690 | Common:1; Rare:23 | ||||
| chr11:14644699-14644725 | Rare:11 | ||||
| chr11:14891627-14891719 | Rare:33 | ||||
| chr11:14892190-14892271 | Rare:36 | ||||
| chr11:16738436-16738857 | Common:3; Rare:104 | ||||
| chr11:17077607-17077968 | Common:2; Rare:150 | ||||
| chr11:17207920-17208111 | Common:1; Rare:72 | ||||
| chr11:17276566-17276828 | Common:4; Rare:68; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17476758-17476931 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:18012903-18013246 | Common:6; Rare:114 |