| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34438769-34438961 | Common:1; Rare:58 | ||||
| chr11:34890549-34890773 | Common:2; Rare:48 | ||||
| chr11:34916251-34916453 | Common:4; Rare:78; Clinvar:4; Clinvar (benign):4 | ||||
| chr11:34916462-34916755 | Common:9; Rare:119; Clinvar:4; Clinvar (benign):10 | ||||
| chr11:35139050-35139169 | Common:1; Rare:24 | ||||
| chr11:35525587-35525752 | Rare:47 | ||||
| chr11:35618262-35618459 | Common:1; Rare:62 | ||||
| chr11:35619375-35619502 | Rare:50 | ||||
| chr11:35662701-35663066 | Common:2; Rare:111 | ||||
| chr11:35663240-35663517 | Rare:103 | ||||
| chr11:35943886-35944090 | Common:3; Rare:67 | ||||
| chr11:36110004-36110208 | Common:1; Rare:45 | ||||
| chr11:36289314-36289542 | Common:3; Rare:76 | ||||
| chr11:36376273-36376398 | Common:1; Rare:31 | ||||
| chr11:36510236-36510372 | Rare:38 |