| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1840803-1841172 | Common:2; Rare:135; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:1996077-1996431 | Common:3; Rare:130 | ||||
| chr11:2377998-2378110 | Common:2; Rare:31 | ||||
| chr11:3380808-3380970 | Common:3; Rare:22 | ||||
| chr11:3476064-3476138 | Rare:23 | ||||
| chr11:3476963-3477170 | Common:2; Rare:61 | ||||
| chr11:3512118-3512265 | Common:2; Rare:30 | ||||
| chr11:6633948-6634092 | Common:1; Rare:42 | ||||
| chr11:7906278-7906413 | Common:3; Rare:14 | ||||
| chr11:9758150-9758356 | Rare:56 | ||||
| chr11:10509988-10510184 | Common:1; Rare:50 | ||||
| chr11:11920242-11920431 | Common:1; Rare:41 | ||||
| chr11:16604273-16604406 | Rare:27 | ||||
| chr11:16925157-16925351 | Common:1; Rare:33 | ||||
| chr11:16996552-16996660 | Rare:22 |