| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:12086691-12086871 | Common:2; Rare:31 | ||||
| chr11:17147559-17147881 | Rare:55 | ||||
| chr11:26188643-26188808 | Rare:31 | ||||
| chr11:27199556-27199759 | Common:2; Rare:32 | ||||
| chr11:30584751-30585088 | Common:3; Rare:68 | ||||
| chr11:34631329-34631563 | Common:3; Rare:36 | ||||
| chr11:43943649-43943675 | Rare:5 | ||||
| chr11:44732045-44732243 | Common:1; Rare:36 | ||||
| chr11:46273166-46273294 | Common:1; Rare:32 | ||||
| chr11:46274410-46274522 | Rare:15 | ||||
| chr11:46865450-46865602 | Common:1; Rare:23 | ||||
| chr11:47165445-47165555 | Common:8; Rare:45 | ||||
| chr11:47395594-47395810 | Common:1; Rare:34 | ||||
| chr11:47413415-47413683 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):6 | ||||
| chr11:57738374-57738695 | Rare:84 |