| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111661484-111661666 | Common:3; Rare:51 | ||||
| chr9:112333522-112333959 | Common:1; Rare:137 | ||||
| chr9:112379775-112380153 | Common:4; Rare:146 | ||||
| chr9:112717986-112718327 | Common:2; Rare:78 | ||||
| chr9:113221246-113221649 | Common:1; Rare:125 | ||||
| chr9:113275359-113275753 | Common:5; Rare:128; Clinvar (pathogenic):1 | ||||
| chr9:113410242-113410734 | Common:3; Rare:148 | ||||
| chr9:113564778-113565058 | Common:5; Rare:59 | ||||
| chr9:114587600-114587877 | Common:2; Rare:100 | ||||
| chr9:116687196-116687364 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120580132-120580389 | Common:1; Rare:80; Clinvar:3 | ||||
| chr9:120793242-120793538 | Common:2; Rare:108 | ||||
| chr9:120842875-120843089 | Common:1; Rare:78 | ||||
| chr9:120877182-120877458 | Common:1; Rare:88 | ||||
| chr9:121074860-121074969 | Rare:52 |