| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:13009086-13009420 | Common:3; Rare:121 | ||||
| chr11:13463141-13463340 | Common:1; Rare:71 | ||||
| chr11:14520297-14520498 | Rare:67 | ||||
| chr11:14643624-14643690 | Common:1; Rare:27 | ||||
| chr11:16738466-16738796 | Common:3; Rare:75 | ||||
| chr11:17014243-17014330 | Rare:32 | ||||
| chr11:17077608-17077836 | Common:2; Rare:92 | ||||
| chr11:17207852-17208111 | Common:2; Rare:92 | ||||
| chr11:17276557-17276832 | Common:4; Rare:74; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18012925-18012996 | Common:1; Rare:26 | ||||
| chr11:18322099-18322347 | Common:6; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322473-18322613 | Common:2; Rare:58 | ||||
| chr11:18394418-18394628 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr11:18396203-18396410 | Rare:76 | ||||
| chr11:18526824-18527001 | Common:1; Rare:82 |