| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10808888-10809199 | Common:2; Rare:140 | ||||
| chr11:10858023-10858260 | Common:2; Rare:76 | ||||
| chr11:11621989-11622222 | Common:3; Rare:90 | ||||
| chr11:11841655-11842054 | Common:4; Rare:122 | ||||
| chr11:12377474-12377623 | Rare:55 | ||||
| chr11:13463170-13463341 | Common:1; Rare:64 | ||||
| chr11:14499798-14499892 | Common:2; Rare:35 | ||||
| chr11:14520303-14520558 | Rare:85 | ||||
| chr11:14643631-14643699 | Common:1; Rare:31 | ||||
| chr11:16738438-16738729 | Common:3; Rare:66 | ||||
| chr11:17077618-17077885 | Common:2; Rare:115 | ||||
| chr11:17207922-17208102 | Common:1; Rare:67 | ||||
| chr11:17276566-17276823 | Common:4; Rare:67; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18322167-18322295 | Common:1; Rare:38 | ||||
| chr11:18322521-18322604 | Common:1; Rare:39 |