| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111599781-111600041 | Common:3; Rare:63 | ||||
| chr9:111631137-111631314 | Rare:35 | ||||
| chr9:111896665-111896821 | Common:2; Rare:56 | ||||
| chr9:112333480-112333968 | Common:1; Rare:144 | ||||
| chr9:112379793-112380163 | Common:4; Rare:144 | ||||
| chr9:113221230-113221633 | Common:1; Rare:129 | ||||
| chr9:113275392-113275734 | Common:5; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:113375486-113375912 | Common:5; Rare:67 | ||||
| chr9:113376474-113376621 | Common:13; Rare:32 | ||||
| chr9:113376728-113376768 | Common:1; Rare:7 | ||||
| chr9:113376790-113377093 | Common:8; Rare:86 | ||||
| chr9:113401241-113401574 | Common:6; Rare:120; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:114094247-114094434 | Common:1; Rare:55 | ||||
| chr9:114387952-114388111 | Common:1; Rare:50 | ||||
| chr9:114505407-114505594 | Common:1; Rare:56 |