| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113056674-113056883 | Rare:72 | ||||
| chr9:113221235-113221584 | Common:1; Rare:113 | ||||
| chr9:113275380-113275734 | Common:5; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:113410289-113410705 | Common:3; Rare:123 | ||||
| chr9:114387943-114388119 | Common:1; Rare:57 | ||||
| chr9:116687217-116687364 | Common:3; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120714465-120714706 | Common:2; Rare:74 | ||||
| chr9:120793244-120793540 | Common:2; Rare:107 | ||||
| chr9:120842867-120843239 | Common:1; Rare:126 | ||||
| chr9:120877168-120877466 | Common:2; Rare:99 | ||||
| chr9:121074827-121074973 | Rare:70 | ||||
| chr9:121075060-121075289 | Rare:58 | ||||
| chr9:121201838-121202149 | Common:2; Rare:89 | ||||
| chr9:121268068-121268207 | Common:1; Rare:45 | ||||
| chr9:121282005-121282103 | Rare:28 |