| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111038665-111038990 | Common:6; Rare:78 | ||||
| chr9:111599346-111599754 | Common:3; Rare:96 | ||||
| chr9:111599793-111599898 | Common:1; Rare:36 | ||||
| chr9:111631113-111631328 | Common:1; Rare:47 | ||||
| chr9:111661481-111661698 | Common:3; Rare:60 | ||||
| chr9:111896656-111896815 | Common:2; Rare:60 | ||||
| chr9:112379800-112380150 | Common:3; Rare:141 | ||||
| chr9:112718016-112718174 | Common:2; Rare:41 | ||||
| chr9:113056649-113056883 | Common:1; Rare:77; Clinvar:1 | ||||
| chr9:113150641-113151041 | Common:5; Rare:95 | ||||
| chr9:113221235-113221640 | Common:1; Rare:129 | ||||
| chr9:113275359-113275728 | Common:5; Rare:118; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340428 | Common:3; Rare:48 | ||||
| chr9:113401241-113401545 | Common:6; Rare:114; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410205-113410737 | Common:3; Rare:169 |