| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10450606-10451049 | Common:8; Rare:212 | ||||
| chr11:10451190-10451374 | Rare:31 | ||||
| chr11:10454986-10455108 | Common:1; Rare:26 | ||||
| chr11:10455122-10455441 | Common:5; Rare:56; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10455905-10456067 | Rare:25 | ||||
| chr11:10541068-10541357 | Common:1; Rare:99 | ||||
| chr11:10633410-10633631 | Common:2; Rare:34 | ||||
| chr11:10651872-10652216 | Common:4; Rare:102 | ||||
| chr11:10750870-10751046 | Common:3; Rare:53 | ||||
| chr11:10751071-10751340 | Rare:83 | ||||
| chr11:10808511-10808715 | Rare:71 | ||||
| chr11:10808865-10809247 | Common:4; Rare:163 | ||||
| chr11:10857296-10857429 | Rare:35 | ||||
| chr11:10858002-10858469 | Common:4; Rare:139 | ||||
| chr11:11621976-11622291 | Common:5; Rare:115 |