| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34438763-34439038 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr11:34916270-34916719 | Common:11; Rare:182; Clinvar:8; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35138954-35139310 | Common:1; Rare:94 | ||||
| chr11:35617761-35618022 | Rare:56 | ||||
| chr11:35662755-35663334 | Common:2; Rare:191 | ||||
| chr11:35943917-35944136 | Common:3; Rare:71 | ||||
| chr11:36377592-36377757 | Common:1; Rare:33 | ||||
| chr11:36455741-36456028 | Rare:60 | ||||
| chr11:36510229-36510372 | Rare:43 | ||||
| chr11:43358831-43358983 | Rare:76 | ||||
| chr11:43680445-43680828 | Common:2; Rare:106 | ||||
| chr11:44066193-44066530 | Common:3; Rare:84 | ||||
| chr11:44565275-44565585 | Common:3; Rare:78 | ||||
| chr11:45804258-45804461 | Common:1; Rare:45 | ||||
| chr11:45804955-45805186 | Common:3; Rare:57; Clinvar:4; Clinvar (benign):1 |