| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113221219-113221662 | Common:2; Rare:271 | ||||
| chr9:113275363-113275734 | Common:10; Rare:230; Clinvar (pathogenic):2 | ||||
| chr9:113303020-113303510 | Common:8; Rare:161 | ||||
| chr9:113340230-113340570 | Common:8; Rare:126 | ||||
| chr9:113376878-113377151 | Common:17; Rare:160 | ||||
| chr9:113401215-113401549 | Common:6; Rare:121; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410270-113410802 | Common:8; Rare:309 | ||||
| chr9:113463575-113463790 | Common:3; Rare:151 | ||||
| chr9:113504935-113505347 | Common:3; Rare:78 | ||||
| chr9:114078090-114078560 | Common:6; Rare:212 | ||||
| chr9:114099241-114099515 | Common:3; Rare:107 | ||||
| chr9:114099600-114100020 | Common:4; Rare:104 | ||||
| chr9:114329160-114329400 | Common:8; Rare:39 | ||||
| chr9:114587443-114587896 | Common:6; Rare:254 | ||||
| chr9:114611226-114611470 | Common:4; Rare:118 |