| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:105447972-105448144 | Common:2; Rare:61 | ||||
| chr9:105558082-105558170 | Rare:21; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106863536-106863642 | Rare:21 | ||||
| chr9:107283403-107283634 | Common:3; Rare:55 | ||||
| chr9:108933931-108934493 | Common:9; Rare:221; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:109013438-109013710 | Common:2; Rare:98 | ||||
| chr9:109498259-109498386 | Rare:44 | ||||
| chr9:110125345-110125563 | Rare:44 | ||||
| chr9:110256410-110256720 | Common:4; Rare:108 | ||||
| chr9:111484221-111484507 | Rare:156 | ||||
| chr9:111599383-111599664 | Common:1; Rare:65 | ||||
| chr9:111631113-111631515 | Common:3; Rare:118 | ||||
| chr9:111661487-111661691 | Common:3; Rare:59 | ||||
| chr9:111896665-111896758 | Common:2; Rare:30 | ||||
| chr9:112332938-112333094 | Rare:46 |