| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:178993-179083 | Common:1; Rare:14 | ||||
| chr9:3526370-3526520 | Common:5; Rare:77 | ||||
| chr9:4679458-4679719 | Common:1; Rare:113 | ||||
| chr9:4741084-4741362 | Common:3; Rare:127 | ||||
| chr9:5437832-5437982 | Common:1; Rare:53 | ||||
| chr9:6757865-6758087 | Common:5; Rare:83 | ||||
| chr9:15422621-15422886 | Common:1; Rare:113 | ||||
| chr9:19127417-19127698 | Common:6; Rare:83 | ||||
| chr9:19380190-19380350 | Common:4; Rare:77 | ||||
| chr9:20684050-20684282 | Common:4; Rare:91 | ||||
| chr9:21994350-21994636 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):4 | ||||
| chr9:26892738-26892895 | Common:1; Rare:77 | ||||
| chr9:26947150-26947369 | Rare:70 | ||||
| chr9:32573082-32573267 | Common:3; Rare:70 | ||||
| chr9:33001561-33001752 | Common:3; Rare:92; Clinvar (benign):3 |