| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127612047-127612403 | Common:2; Rare:130; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:127803176-127803353 | Rare:36 | ||||
| chr9:127807924-127808211 | Common:3; Rare:58 | ||||
| chr9:127854438-127854625 | Rare:50; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:127854642-127854673 | Rare:11; Clinvar:1 | ||||
| chr9:127897406-127897557 | Common:1; Rare:41 | ||||
| chr9:127899504-127899742 | Rare:85 | ||||
| chr9:127916844-127917261 | Common:1; Rare:104 | ||||
| chr9:128091331-128091472 | Rare:28 | ||||
| chr9:128098361-128098561 | Common:1; Rare:47 | ||||
| chr9:128100807-128101022 | Common:2; Rare:39 | ||||
| chr9:128190351-128190555 | Rare:61 | ||||
| chr9:128191424-128191679 | Rare:73 | ||||
| chr9:128191745-128191858 | Common:1; Rare:30 | ||||
| chr9:128275191-128275380 | Common:1; Rare:42 |