| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122931470-122931698 | Common:3; Rare:49 | ||||
| chr9:124861905-124862134 | Common:1; Rare:96 | ||||
| chr9:124940975-124941184 | Common:3; Rare:73 | ||||
| chr9:125189738-125190050 | Common:1; Rare:137 | ||||
| chr9:125241013-125241097 | Rare:30 | ||||
| chr9:125241255-125241393 | Common:1; Rare:48 | ||||
| chr9:127122606-127122865 | Common:3; Rare:66 | ||||
| chr9:127424260-127424440 | Common:1; Rare:58 | ||||
| chr9:127451391-127451523 | Rare:39 | ||||
| chr9:127579004-127579217 | Common:3; Rare:36 | ||||
| chr9:127612018-127612356 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127854451-127854788 | Rare:81; Clinvar:8; Clinvar (benign):4 | ||||
| chr9:128275903-128276293 | Common:4; Rare:171 | ||||
| chr9:128371233-128371401 | Rare:65 | ||||
| chr9:128552433-128552614 | Rare:75; Clinvar:1 |