| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136665492-136665814 | Common:2; Rare:83 | ||||
| chr9:136848659-136848795 | Rare:38 | ||||
| chr9:136849637-136849772 | Common:1; Rare:49 | ||||
| chr9:136886249-136886533 | Common:2; Rare:83 | ||||
| chr9:137086609-137087146 | Common:2; Rare:222; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137188537-137188713 | Common:2; Rare:84 | ||||
| chr9:137205422-137205763 | Common:1; Rare:128 | ||||
| chr9:137618797-137619046 | Common:1; Rare:113 | ||||
| chrM:3168-3436 | |||||
| chrM:3560-3607 | |||||
| chrM:4320-4578 | |||||
| chrM:5576-5757 | |||||
| chrM:5823-5997 | |||||
| chrM:6169-6264 | |||||
| chrM:6277-6321 |