| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113056550-113057000 | Common:3; Rare:222; Clinvar:1 | ||||
| chr9:113221205-113221662 | Common:2; Rare:276 | ||||
| chr9:113275359-113275837 | Common:10; Rare:268; Clinvar (pathogenic):2 | ||||
| chr9:113340212-113340456 | Common:6; Rare:112 | ||||
| chr9:113376876-113377096 | Common:15; Rare:129 | ||||
| chr9:113401215-113401559 | Common:6; Rare:123; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410272-113410826 | Common:8; Rare:326 | ||||
| chr9:113463430-113463809 | Common:5; Rare:192 | ||||
| chr9:114155428-114155552 | Rare:34 | ||||
| chr9:114505434-114505561 | Common:1; Rare:42 | ||||
| chr9:114587551-114587859 | Common:5; Rare:232 | ||||
| chr9:114611213-114611478 | Common:3; Rare:95 | ||||
| chr9:114611630-114612170 | Common:6; Rare:167 | ||||
| chr9:114805629-114805729 | Rare:11 | ||||
| chr9:114806035-114806184 | Rare:56 |