| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35205508-35205839 | Rare:54 | ||||
| chr11:35617657-35618057 | Common:1; Rare:78 | ||||
| chr11:35618297-35618582 | Common:1; Rare:101 | ||||
| chr11:35619101-35619522 | Common:1; Rare:146 | ||||
| chr11:35663227-35663605 | Rare:141; Clinvar (pathogenic):1 | ||||
| chr11:36376459-36376664 | Common:1; Rare:41 | ||||
| chr11:36510202-36510414 | Rare:76 | ||||
| chr11:36510632-36510675 | Rare:7 | ||||
| chr11:43358795-43359107 | Rare:129 | ||||
| chr11:43680367-43680982 | Common:6; Rare:176 | ||||
| chr11:43880724-43880978 | Common:3; Rare:65 | ||||
| chr11:43881155-43881174 | Rare:3 | ||||
| chr11:44066418-44066550 | Common:2; Rare:34 | ||||
| chr11:44565551-44565750 | Common:1; Rare:56 | ||||
| chr11:45804972-45805212 | Common:3; Rare:65; Clinvar:4; Clinvar (benign):1 |