| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34358005-34358262 | Common:2; Rare:71 | ||||
| chr11:34438776-34439023 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr11:34916282-34916756 | Common:13; Rare:194; Clinvar:8; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr11:35138736-35138869 | Common:1; Rare:33 | ||||
| chr11:35139023-35139348 | Common:1; Rare:84 | ||||
| chr11:35139666-35139713 | Rare:11 | ||||
| chr11:35662634-35663345 | Common:3; Rare:226 | ||||
| chr11:35943857-35944131 | Common:3; Rare:90 | ||||
| chr11:36289370-36289505 | Common:1; Rare:54 | ||||
| chr11:36510229-36510377 | Rare:45 | ||||
| chr11:43358790-43358983 | Rare:92 | ||||
| chr11:43644168-43644247 | Rare:11 | ||||
| chr11:43880701-43881114 | Common:5; Rare:94 | ||||
| chr11:44066105-44066349 | Common:3; Rare:61 | ||||
| chr11:45804974-45805186 | Common:3; Rare:53; Clinvar:4; Clinvar (benign):1 |