| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108934006-108934477 | Common:7; Rare:184; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109498233-109498381 | Rare:49 | ||||
| chr9:110256422-110256718 | Common:4; Rare:104 | ||||
| chr9:111661487-111661644 | Common:2; Rare:42 | ||||
| chr9:112379793-112380157 | Common:4; Rare:143 | ||||
| chr9:113056674-113056866 | Rare:65 | ||||
| chr9:113221262-113221594 | Rare:106 | ||||
| chr9:113275392-113275726 | Common:5; Rare:110; Clinvar (pathogenic):1 | ||||
| chr9:113349463-113349752 | Rare:108 | ||||
| chr9:113410290-113410705 | Common:3; Rare:122 | ||||
| chr9:114094255-114094336 | Rare:28 | ||||
| chr9:114099272-114099416 | Common:1; Rare:30 | ||||
| chr9:114387983-114388108 | Common:1; Rare:43 | ||||
| chr9:114505459-114505566 | Common:1; Rare:39 | ||||
| chr9:116687196-116687361 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):1 |