| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113187994-113188189 | Common:2; Rare:26 | ||||
| chr9:113221235-113221633 | Common:1; Rare:128 | ||||
| chr9:113275359-113275728 | Common:5; Rare:118; Clinvar (pathogenic):1 | ||||
| chr9:113376877-113377134 | Common:9; Rare:81 | ||||
| chr9:113410226-113410714 | Common:3; Rare:143 | ||||
| chr9:114387949-114388119 | Common:1; Rare:53 | ||||
| chr9:114587600-114587910 | Common:2; Rare:114 | ||||
| chr9:116687207-116687361 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120714465-120714706 | Common:2; Rare:74 | ||||
| chr9:120793248-120793538 | Common:2; Rare:107 | ||||
| chr9:120842905-120843283 | Common:1; Rare:121 | ||||
| chr9:120868827-120869060 | Common:2; Rare:50 | ||||
| chr9:120877178-120877447 | Common:1; Rare:83 | ||||
| chr9:120929086-120929141 | Common:1; Rare:12 | ||||
| chr9:121074821-121074977 | Rare:75 |