| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:109118514-109118715 | Rare:42 | ||||
| chr9:109295037-109295196 | Common:1; Rare:29 | ||||
| chr9:110123916-110124015 | Common:1; Rare:17 | ||||
| chr9:111039198-111039453 | Common:2; Rare:51 | ||||
| chr9:112073409-112073581 | Common:2; Rare:38 | ||||
| chr9:113273374-113273586 | Common:2; Rare:31 | ||||
| chr9:113583370-113583503 | Rare:46 | ||||
| chr9:114387235-114387311 | Rare:17 | ||||
| chr9:114398452-114398687 | Common:2; Rare:61 | ||||
| chr9:120524954-120525296 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:120527834-120528128 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120733213-120733389 | Rare:29 | ||||
| chr9:121310547-121310845 | Common:1; Rare:81; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:121312153-121312488 | Common:1; Rare:100; Clinvar:1 | ||||
| chr9:121318402-121318907 | Common:1; Rare:147; Clinvar:2; Clinvar (benign):2 |