| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100352858-100353096 | Rare:87 | ||||
| chr9:100427004-100427379 | Common:7; Rare:133 | ||||
| chr9:101398594-101398907 | Common:1; Rare:98 | ||||
| chr9:104747512-104747763 | Rare:65 | ||||
| chr9:105558024-105558153 | Rare:43 | ||||
| chr9:107283097-107283284 | Common:1; Rare:59 | ||||
| chr9:108933925-108934477 | Common:9; Rare:214; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:110207526-110207703 | Rare:59 | ||||
| chr9:111631181-111631374 | Common:1; Rare:54 | ||||
| chr9:112175269-112175352 | Rare:17 | ||||
| chr9:112332953-112333137 | Common:1; Rare:58 | ||||
| chr9:112379845-112380138 | Common:2; Rare:121 | ||||
| chr9:113221228-113221591 | Common:1; Rare:119 | ||||
| chr9:113275382-113275734 | Common:5; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340380 | Common:2; Rare:36 |