| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:102529037-102529132 | Rare:25 | ||||
| chr8:103501920-103502181 | Common:3; Rare:55 | ||||
| chr8:131041528-131041665 | Common:1; Rare:30 | ||||
| chr8:143039229-143039277 | Rare:11 | ||||
| chr8:143281636-143281799 | Common:3; Rare:40 | ||||
| chr8:144093619-144093806 | Rare:22 | ||||
| chr8:144700364-144700694 | Common:3; Rare:75 | ||||
| chr8:145002825-145003043 | Common:2; Rare:78 | ||||
| chr9:9441755-9442067 | Common:4; Rare:83 | ||||
| chr9:14316955-14317107 | Rare:34 | ||||
| chr9:14993148-14993318 | Common:5; Rare:73 | ||||
| chr9:32550831-32551121 | Common:1; Rare:119; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33818759-33818787 | Rare:3 | ||||
| chr9:37079574-37079943 | Common:4; Rare:87 | ||||
| chr9:39464450-39464657 | Common:1; Rare:50 |