| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:576413-576584 | Rare:71 | ||||
| chr11:613582-613770 | Common:11; Rare:69 | ||||
| chr11:615946-616042 | Common:1; Rare:29 | ||||
| chr11:695746-695821 | Rare:26 | ||||
| chr11:763151-763509 | Common:23; Rare:180; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr11:764038-764418 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:777451-777598 | Common:1; Rare:66 | ||||
| chr11:798008-798353 | Common:3; Rare:124 | ||||
| chr11:805196-805310 | Common:4; Rare:48 | ||||
| chr11:809516-810171 | Common:6; Rare:225 | ||||
| chr11:832833-833020 | Common:7; Rare:63 | ||||
| chr11:842458-842978 | Common:8; Rare:216 | ||||
| chr11:843965-844141 | Common:1; Rare:43 | ||||
| chr11:925663-926004 | Common:3; Rare:145 | ||||
| chr11:1006256-1006574 | Common:1; Rare:80 |