| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101487092-101487257 | Common:3; Rare:34 | ||||
| chr9:101533743-101533905 | Rare:53 | ||||
| chr9:104093977-104094350 | Common:3; Rare:93 | ||||
| chr9:104747608-104747795 | Common:1; Rare:58 | ||||
| chr9:104764097-104764201 | Common:2; Rare:28 | ||||
| chr9:104928145-104928504 | Common:6; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:105447927-105448153 | Common:4; Rare:85 | ||||
| chr9:105558060-105558170 | Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862405-106862735 | Common:4; Rare:84 | ||||
| chr9:106862901-106863186 | Rare:85 | ||||
| chr9:107283080-107283284 | Common:1; Rare:67 | ||||
| chr9:107283403-107283621 | Common:3; Rare:54 | ||||
| chr9:108933917-108934516 | Common:10; Rare:236; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:110048527-110048716 | Common:1; Rare:56 | ||||
| chr9:111484212-111484356 | Rare:66 |