| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127735274-127735542 | Common:1; Rare:73 | ||||
| chr9:127742652-127742844 | Rare:41 | ||||
| chr9:127755142-127755439 | Common:1; Rare:73 | ||||
| chr9:127778660-127778940 | Common:1; Rare:55 | ||||
| chr9:127784909-127785309 | Common:2; Rare:136 | ||||
| chr9:127786540-127786840 | Common:3; Rare:103 | ||||
| chr9:127802716-127802944 | Common:2; Rare:50 | ||||
| chr9:127802990-127803340 | Common:3; Rare:96 | ||||
| chr9:127873439-127873608 | Common:1; Rare:46 | ||||
| chr9:127897310-127897600 | Common:1; Rare:63 | ||||
| chr9:127899578-127899720 | Rare:55 | ||||
| chr9:127916974-127917308 | Common:1; Rare:97 | ||||
| chr9:127937788-127937981 | Common:2; Rare:62; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:127950660-127951020 | Common:1; Rare:74 | ||||
| chr9:127980955-127981382 | Common:3; Rare:129 |