| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112718002-112718351 | Common:2; Rare:83 | ||||
| chr9:113056671-113056883 | Rare:73 | ||||
| chr9:113221257-113221589 | Common:1; Rare:107 | ||||
| chr9:113275380-113275728 | Common:5; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:113376974-113377057 | Common:6; Rare:32 | ||||
| chr9:113401263-113401545 | Common:6; Rare:104; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410289-113410817 | Common:4; Rare:171 | ||||
| chr9:113517218-113517325 | Rare:33 | ||||
| chr9:113580650-113580943 | Common:4; Rare:49 | ||||
| chr9:114387983-114388119 | Common:1; Rare:45 | ||||
| chr9:114587588-114587856 | Common:2; Rare:100 | ||||
| chr9:114611220-114611560 | Common:4; Rare:110 | ||||
| chr9:114930140-114930187 | Common:1; Rare:10 | ||||
| chr9:114930278-114930296 | Rare:5 | ||||
| chr9:114930480-114930701 | Common:4; Rare:55 |