| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9460611-9461037 | Common:4; Rare:111 | ||||
| chr11:9663884-9664182 | Common:4; Rare:95 | ||||
| chr11:10751163-10751289 | Rare:38 | ||||
| chr11:10808858-10809204 | Common:3; Rare:153 | ||||
| chr11:10858013-10858260 | Common:3; Rare:81 | ||||
| chr11:11841933-11842069 | Common:1; Rare:37 | ||||
| chr11:12377488-12377643 | Rare:63 | ||||
| chr11:13463093-13463395 | Common:1; Rare:107 | ||||
| chr11:14499782-14500110 | Common:3; Rare:84 | ||||
| chr11:16738466-16738723 | Common:3; Rare:55 | ||||
| chr11:17077606-17077847 | Common:2; Rare:100 | ||||
| chr11:17207919-17208082 | Common:1; Rare:62 | ||||
| chr11:17276566-17276818 | Common:3; Rare:67; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:18106011-18106308 | Common:2; Rare:100 | ||||
| chr11:18322075-18322332 | Common:5; Rare:98; Clinvar:2; Clinvar (benign):2 |