| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104928187-104928517 | Common:5; Rare:83; Clinvar (benign):1 | ||||
| chr9:105244319-105244648 | Common:1; Rare:120 | ||||
| chr9:105447955-105448144 | Common:2; Rare:68 | ||||
| chr9:105558067-105558170 | Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:105694406-105694627 | Common:3; Rare:97 | ||||
| chr9:106862990-106863180 | Rare:65 | ||||
| chr9:107282945-107283284 | Common:3; Rare:119 | ||||
| chr9:108933945-108934001 | Common:1; Rare:24; Clinvar:4 | ||||
| chr9:108934032-108934493 | Common:7; Rare:183; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109013445-109013729 | Common:2; Rare:101 | ||||
| chr9:109498246-109498423 | Rare:61 | ||||
| chr9:110125345-110125563 | Rare:44 | ||||
| chr9:110256410-110256729 | Common:5; Rare:110 | ||||
| chr9:110256902-110257056 | Rare:35 | ||||
| chr9:111484138-111484423 | Common:1; Rare:129 |