| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10455116-10455279 | Common:2; Rare:25; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:10455329-10455414 | Common:3; Rare:17; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:10456263-10456327 | Rare:15 | ||||
| chr11:10540490-10540555 | Rare:14 | ||||
| chr11:10540568-10540762 | Common:2; Rare:45 | ||||
| chr11:10540841-10541374 | Common:1; Rare:165 | ||||
| chr11:10594477-10594744 | Common:3; Rare:49 | ||||
| chr11:10750867-10751066 | Common:3; Rare:58 | ||||
| chr11:10751071-10751367 | Rare:89 | ||||
| chr11:10807827-10808283 | Common:1; Rare:160 | ||||
| chr11:10808401-10809294 | Common:6; Rare:339 | ||||
| chr11:10809364-10809784 | Common:1; Rare:99 | ||||
| chr11:10856681-10857008 | Common:2; Rare:52 | ||||
| chr11:10857294-10857445 | Rare:38 | ||||
| chr11:10857708-10857925 | Common:2; Rare:53 |