| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10858019-10858269 | Common:3; Rare:81 | ||||
| chr11:11841940-11842097 | Common:1; Rare:42 | ||||
| chr11:12008568-12008839 | Common:2; Rare:58 | ||||
| chr11:13463134-13463570 | Common:2; Rare:139 | ||||
| chr11:13668342-13668762 | Common:1; Rare:136 | ||||
| chr11:14520313-14520549 | Rare:76 | ||||
| chr11:14891637-14891798 | Rare:43 | ||||
| chr11:16607662-16607960 | Common:1; Rare:39 | ||||
| chr11:16738456-16738723 | Common:3; Rare:56 | ||||
| chr11:17077618-17077885 | Common:2; Rare:115 | ||||
| chr11:17207911-17208111 | Common:2; Rare:75 | ||||
| chr11:17276572-17276809 | Common:3; Rare:59; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:18012990-18013248 | Common:5; Rare:82 | ||||
| chr11:18322158-18322314 | Common:1; Rare:49 | ||||
| chr11:18322474-18322610 | Common:2; Rare:58 |