| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111631137-111631375 | Common:1; Rare:67 | ||||
| chr9:113221247-113221607 | Common:1; Rare:114 | ||||
| chr9:116687228-116687364 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793371-120793492 | Rare:44 | ||||
| chr9:121201859-121202161 | Common:2; Rare:82 | ||||
| chr9:121370217-121370534 | Common:1; Rare:86 | ||||
| chr9:122264814-122264919 | Common:1; Rare:28 | ||||
| chr9:122931498-122931698 | Common:3; Rare:43 | ||||
| chr9:125240691-125241153 | Rare:123 | ||||
| chr9:125241201-125241400 | Common:2; Rare:67 | ||||
| chr9:127451375-127451523 | Common:1; Rare:50 | ||||
| chr9:127579029-127579293 | Common:4; Rare:57 | ||||
| chr9:127916972-127917261 | Common:1; Rare:88 | ||||
| chr9:128275903-128276293 | Common:4; Rare:171 | ||||
| chr9:128552414-128552603 | Rare:74; Clinvar:1 |