| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97633528-97633829 | Common:4; Rare:94 | ||||
| chr9:97922440-97922598 | Common:3; Rare:83 | ||||
| chr9:98255349-98255476 | Common:1; Rare:43 | ||||
| chr9:98255557-98255818 | Common:3; Rare:77 | ||||
| chr9:99221895-99222349 | Common:2; Rare:177; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:100098936-100099272 | Common:2; Rare:89 | ||||
| chr9:100352885-100352996 | Rare:36 | ||||
| chr9:101398591-101398890 | Common:1; Rare:97 | ||||
| chr9:105558040-105558153 | Rare:36 | ||||
| chr9:108934074-108934484 | Common:7; Rare:165; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110579126-110579336 | Rare:58 | ||||
| chr9:111631137-111631386 | Common:1; Rare:69 | ||||
| chr9:112379841-112380146 | Common:3; Rare:126 | ||||
| chr9:113221230-113221598 | Common:1; Rare:118 | ||||
| chr9:113275382-113275697 | Common:5; Rare:91; Clinvar (pathogenic):1 |