| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108933951-108933985 | Common:1; Rare:12; Clinvar:3 | ||||
| chr9:108934069-108934477 | Common:7; Rare:162; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110048530-110048776 | Common:2; Rare:89 | ||||
| chr9:110256410-110256725 | Common:5; Rare:109 | ||||
| chr9:110579539-110579600 | Common:1; Rare:21 | ||||
| chr9:110579877-110580084 | Common:1; Rare:46 | ||||
| chr9:110580086-110580125 | Rare:9 | ||||
| chr9:112379848-112380165 | Common:2; Rare:130 | ||||
| chr9:113056657-113056909 | Common:1; Rare:81; Clinvar:1 | ||||
| chr9:113221229-113221628 | Common:1; Rare:127 | ||||
| chr9:113275359-113275746 | Common:5; Rare:125; Clinvar (pathogenic):1 | ||||
| chr9:113340243-113340431 | Common:3; Rare:47 | ||||
| chr9:113410295-113410719 | Common:3; Rare:123 | ||||
| chr9:114587448-114587884 | Common:4; Rare:156 | ||||
| chr9:116687228-116687364 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):1 |