| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122264723-122264922 | Common:2; Rare:56 | ||||
| chr9:122375176-122375351 | Common:3; Rare:51 | ||||
| chr9:122905044-122905126 | Rare:23 | ||||
| chr9:122905220-122905535 | Common:2; Rare:120 | ||||
| chr9:122931482-122931694 | Common:3; Rare:44 | ||||
| chr9:124861903-124862103 | Rare:86 | ||||
| chr9:124940956-124941184 | Common:3; Rare:85 | ||||
| chr9:125189725-125190037 | Common:1; Rare:142 | ||||
| chr9:125200287-125200590 | Common:1; Rare:102 | ||||
| chr9:125241374-125241676 | Common:2; Rare:80 | ||||
| chr9:125261657-125261860 | Common:2; Rare:74 | ||||
| chr9:125747543-125747651 | Rare:37 | ||||
| chr9:127122613-127123102 | Common:3; Rare:144 | ||||
| chr9:127424337-127424467 | Common:1; Rare:38 | ||||
| chr9:127451244-127451562 | Common:3; Rare:132; Clinvar (benign):1 |