| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:126860589-126860693 | Common:2; Rare:34 | ||||
| chr9:127122662-127122970 | Common:3; Rare:80 | ||||
| chr9:127245190-127245341 | Common:1; Rare:37 | ||||
| chr9:127424111-127424489 | Common:1; Rare:109 | ||||
| chr9:127451267-127451565 | Common:3; Rare:123; Clinvar (benign):1 | ||||
| chr9:127612000-127612434 | Common:2; Rare:156; Clinvar:5; Clinvar (benign):5 | ||||
| chr9:127762412-127762557 | Common:1; Rare:29 | ||||
| chr9:127778687-127778854 | Common:1; Rare:28 | ||||
| chr9:127788057-127788385 | Common:2; Rare:101 | ||||
| chr9:127802708-127803032 | Common:3; Rare:89 | ||||
| chr9:127803792-127804179 | Common:3; Rare:70 | ||||
| chr9:127854613-127854839 | Rare:45; Clinvar:5 | ||||
| chr9:127873460-127873579 | Rare:35 | ||||
| chr9:127874617-127874760 | Rare:32 | ||||
| chr9:127877667-127877767 | Rare:18 |