| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127424255-127424475 | Common:1; Rare:72 | ||||
| chr9:127449279-127449460 | Common:2; Rare:53 | ||||
| chr9:127451263-127451557 | Common:3; Rare:123; Clinvar (benign):1 | ||||
| chr9:127612047-127612434 | Common:2; Rare:139; Clinvar:5; Clinvar (benign):5 | ||||
| chr9:127778710-127778972 | Common:1; Rare:48 | ||||
| chr9:127877645-127877767 | Rare:29 | ||||
| chr9:127930759-127930971 | Common:3; Rare:52 | ||||
| chr9:127937816-127937932 | Common:1; Rare:32; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:128091296-128091511 | Rare:44 | ||||
| chr9:128091670-128091872 | Common:4; Rare:36 | ||||
| chr9:128160024-128160478 | Common:2; Rare:108 | ||||
| chr9:128191344-128191642 | Rare:85 | ||||
| chr9:128191753-128191870 | Common:1; Rare:30 | ||||
| chr9:128218724-128219053 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:128275929-128276302 | Common:5; Rare:171 |