| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122913268-122913395 | Common:2; Rare:24 | ||||
| chr9:122931464-122931680 | Common:3; Rare:42 | ||||
| chr9:124861908-124862136 | Common:1; Rare:95 | ||||
| chr9:124940957-124941184 | Common:3; Rare:84 | ||||
| chr9:125189715-125190027 | Common:1; Rare:141 | ||||
| chr9:125241282-125241656 | Common:2; Rare:112 | ||||
| chr9:126804928-126805075 | Common:3; Rare:46 | ||||
| chr9:127122608-127122994 | Common:3; Rare:107 | ||||
| chr9:127424081-127424458 | Common:1; Rare:110 | ||||
| chr9:127449614-127449835 | Rare:56 | ||||
| chr9:127451280-127451592 | Common:3; Rare:122; Clinvar (benign):1 | ||||
| chr9:127612018-127612379 | Common:2; Rare:130; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:127762292-127762557 | Common:2; Rare:60 | ||||
| chr9:127854312-127854567 | Common:2; Rare:66; Clinvar:5; Clinvar (benign):7 | ||||
| chr9:127877624-127877791 | Rare:39 |