| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35403540-35403950 | Common:13; Rare:51 | ||||
| chr11:35404422-35404880 | Common:17; Rare:167 | ||||
| chr11:35549743-35550251 | Common:7; Rare:189 | ||||
| chr11:35553938-35554093 | Common:3; Rare:29 | ||||
| chr11:35663330-35663880 | Common:2; Rare:331; Clinvar (pathogenic):2 | ||||
| chr11:35953090-35953400 | Common:3; Rare:56 | ||||
| chr11:36018984-36019384 | Common:6; Rare:144 | ||||
| chr11:37088100-37088526 | Common:2; Rare:85 | ||||
| chr11:38460900-38461230 | Rare:181 | ||||
| chr11:38811483-38811782 | Common:4; Rare:74 | ||||
| chr11:43738980-43739330 | Common:6; Rare:84 | ||||
| chr11:44143954-44144238 | Rare:53 | ||||
| chr11:44190770-44191150 | Rare:69 | ||||
| chr11:44316830-44317370 | Common:4; Rare:116 | ||||
| chr11:44577048-44577634 | Common:4; Rare:216 |