| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10455124-10455287 | Common:2; Rare:26; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:10455861-10456107 | Rare:40 | ||||
| chr11:10456192-10456395 | Rare:48 | ||||
| chr11:10456418-10456697 | Common:1; Rare:53 | ||||
| chr11:10541082-10541325 | Common:1; Rare:87 | ||||
| chr11:10750977-10751460 | Common:1; Rare:147 | ||||
| chr11:10807773-10807917 | Rare:36 | ||||
| chr11:10808454-10808686 | Rare:87 | ||||
| chr11:10808709-10809445 | Common:8; Rare:267 | ||||
| chr11:10809499-10809715 | Rare:49 | ||||
| chr11:10857144-10857460 | Rare:70 | ||||
| chr11:10857712-10857938 | Common:1; Rare:56 | ||||
| chr11:10857962-10858366 | Common:3; Rare:125 | ||||
| chr11:10858609-10858688 | Rare:21 | ||||
| chr11:10858784-10859021 | Common:2; Rare:73 |