| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45147086-45147388 | Common:1; Rare:133 | ||||
| chr11:45286245-45286457 | Rare:55 | ||||
| chr11:45803951-45804091 | Common:1; Rare:26 | ||||
| chr11:45804307-45804466 | Common:1; Rare:33 | ||||
| chr11:45804933-45805217 | Common:3; Rare:75; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45805362-45805581 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:45847126-45847529 | Common:2; Rare:155 | ||||
| chr11:45917817-45918051 | Rare:64; Clinvar:2 | ||||
| chr11:45918054-45918227 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr11:45918730-45918904 | Common:1; Rare:48 | ||||
| chr11:45921556-45921649 | Common:1; Rare:15 | ||||
| chr11:45922005-45922440 | Common:2; Rare:109 | ||||
| chr11:45922494-45922740 | Common:5; Rare:80 | ||||
| chr11:45922857-45922959 | Rare:26 | ||||
| chr11:45923111-45923277 | Common:1; Rare:46 |