| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94128684-94128792 | Rare:38 | ||||
| chr11:94128794-94129628 | Common:7; Rare:279 | ||||
| chr11:94493370-94493468 | Common:2; Rare:26 | ||||
| chr11:94493487-94493654 | Rare:37 | ||||
| chr11:94493740-94494281 | Common:8; Rare:144; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94544195-94544486 | Common:2; Rare:140 | ||||
| chr11:94706061-94706157 | Common:1; Rare:15 | ||||
| chr11:94706298-94706532 | Common:2; Rare:37 | ||||
| chr11:94706571-94706946 | Common:2; Rare:69 | ||||
| chr11:94768058-94768502 | Common:3; Rare:124 | ||||
| chr11:94768767-94769094 | Common:2; Rare:72 | ||||
| chr11:94973498-94973909 | Rare:114 | ||||
| chr11:94973961-94974177 | Rare:31 | ||||
| chr11:95066875-95067014 | Rare:25 | ||||
| chr11:95067018-95067298 | Rare:83 |