| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:126804876-126805060 | Common:1; Rare:58 | ||||
| chr9:126860587-126860707 | Common:2; Rare:41 | ||||
| chr9:127122514-127122551 | Rare:5 | ||||
| chr9:127122602-127123001 | Common:3; Rare:112 | ||||
| chr9:127424249-127424471 | Common:1; Rare:70 | ||||
| chr9:127451274-127451572 | Common:3; Rare:120; Clinvar (benign):1 | ||||
| chr9:127451883-127451962 | Rare:14 | ||||
| chr9:127612018-127612357 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127802748-127802960 | Common:2; Rare:49 | ||||
| chr9:127897347-127897519 | Common:1; Rare:36 | ||||
| chr9:127916989-127917277 | Common:1; Rare:84 | ||||
| chr9:128098289-128098544 | Common:1; Rare:54 | ||||
| chr9:128098761-128099085 | Common:1; Rare:70 | ||||
| chr9:128191468-128191642 | Rare:53 | ||||
| chr9:128191753-128191844 | Common:1; Rare:23 |