| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111599785-111599878 | Common:1; Rare:32 | ||||
| chr9:112379800-112380153 | Common:3; Rare:141 | ||||
| chr9:112718002-112718150 | Common:2; Rare:38 | ||||
| chr9:113056602-113056918 | Common:1; Rare:109; Clinvar:1 | ||||
| chr9:113221221-113221594 | Common:1; Rare:123 | ||||
| chr9:113275392-113275734 | Common:5; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340431 | Common:3; Rare:49 | ||||
| chr9:113410214-113410741 | Common:4; Rare:164 | ||||
| chr9:114587600-114587883 | Common:2; Rare:102 | ||||
| chr9:115118010-115118237 | Common:3; Rare:54 | ||||
| chr9:116687240-116687370 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:119369295-119369793 | Common:2; Rare:114 | ||||
| chr9:120714468-120714732 | Common:2; Rare:88 | ||||
| chr9:120793248-120793533 | Common:1; Rare:104 | ||||
| chr9:120842905-120843100 | Common:1; Rare:68 |