| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:107283403-107283674 | Common:3; Rare:66 | ||||
| chr9:107489767-107490028 | Common:3; Rare:108 | ||||
| chr9:108934029-108934508 | Common:7; Rare:192; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109498246-109498433 | Rare:63 | ||||
| chr9:110125345-110125553 | Rare:42 | ||||
| chr9:110207029-110207282 | Common:2; Rare:31 | ||||
| chr9:110207519-110207563 | Rare:14 | ||||
| chr9:110256411-110256718 | Common:4; Rare:107 | ||||
| chr9:110579379-110579679 | Common:2; Rare:90 | ||||
| chr9:110579762-110579962 | Common:2; Rare:59 | ||||
| chr9:110579984-110580098 | Rare:17 | ||||
| chr9:111038190-111038450 | Common:2; Rare:71 | ||||
| chr9:111631173-111631289 | Rare:19 | ||||
| chr9:111661486-111661673 | Common:3; Rare:55 | ||||
| chr9:112332976-112333111 | Common:1; Rare:41 |