| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33722588-33722857 | Common:2; Rare:58 | ||||
| chr11:33736390-33736584 | Common:2; Rare:63 | ||||
| chr11:34052119-34052539 | Common:4; Rare:190 | ||||
| chr11:34438776-34438998 | Common:2; Rare:74; Clinvar (benign):1 | ||||
| chr11:34916231-34916661 | Common:11; Rare:170; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35138455-35138922 | Common:2; Rare:85 | ||||
| chr11:35139102-35139365 | Rare:74 | ||||
| chr11:35662934-35663500 | Rare:195 | ||||
| chr11:36510222-36510353 | Rare:40 | ||||
| chr11:43358846-43359097 | Rare:100 | ||||
| chr11:43680461-43680982 | Common:2; Rare:155 | ||||
| chr11:43880740-43880884 | Common:2; Rare:29 | ||||
| chr11:44066114-44066351 | Common:3; Rare:58 | ||||
| chr11:44066425-44066530 | Common:2; Rare:29 | ||||
| chr11:45146539-45146671 | Common:1; Rare:26 |