| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92670056-92670369 | Common:1; Rare:94 | ||||
| chr9:98192623-98192883 | Common:6; Rare:70 | ||||
| chr9:99221977-99222329 | Common:2; Rare:121 | ||||
| chr9:99906589-99906684 | Rare:44 | ||||
| chr9:100098979-100099307 | Common:2; Rare:89; Clinvar:1 | ||||
| chr9:100352860-100353050 | Rare:60 | ||||
| chr9:101398587-101398887 | Common:1; Rare:98 | ||||
| chr9:108934094-108934415 | Common:7; Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498253-109498565 | Common:1; Rare:86 | ||||
| chr9:111599639-111599898 | Common:2; Rare:74 | ||||
| chr9:112379798-112380143 | Common:3; Rare:140 | ||||
| chr9:113221294-113221607 | Rare:95 | ||||
| chr9:113275381-113275728 | Common:5; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:113410645-113410793 | Common:2; Rare:52 | ||||
| chr9:113463533-113463753 | Common:2; Rare:67 |