| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111661478-111661691 | Common:3; Rare:60 | ||||
| chr9:111896665-111896760 | Common:2; Rare:30 | ||||
| chr9:112333524-112333949 | Rare:131 | ||||
| chr9:112379759-112380132 | Common:4; Rare:139 | ||||
| chr9:112486652-112486977 | Rare:104 | ||||
| chr9:112487046-112487166 | Common:1; Rare:35 | ||||
| chr9:112717992-112718241 | Common:2; Rare:62 | ||||
| chr9:113055997-113056317 | Rare:54 | ||||
| chr9:113056462-113056883 | Common:1; Rare:151; Clinvar:1 | ||||
| chr9:113150641-113151040 | Common:5; Rare:95 | ||||
| chr9:113221217-113221640 | Common:1; Rare:136 | ||||
| chr9:113275138-113275339 | Rare:54 | ||||
| chr9:113275376-113275755 | Common:5; Rare:125; Clinvar (pathogenic):1 | ||||
| chr9:113340215-113340433 | Common:3; Rare:58 | ||||
| chr9:113376914-113377103 | Common:7; Rare:62 |