| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97013757-97013817 | Rare:13 | ||||
| chr9:97633267-97633892 | Common:7; Rare:191 | ||||
| chr9:97666596-97666826 | Common:1; Rare:43 | ||||
| chr9:97853113-97853287 | Common:2; Rare:57 | ||||
| chr9:97922416-97922600 | Common:4; Rare:91 | ||||
| chr9:97983152-97983590 | Common:2; Rare:166 | ||||
| chr9:97984494-97984600 | Common:1; Rare:55 | ||||
| chr9:98255349-98255426 | Common:1; Rare:26 | ||||
| chr9:98255513-98255830 | Common:3; Rare:93 | ||||
| chr9:98943331-98943897 | Common:4; Rare:140 | ||||
| chr9:99221892-99222360 | Common:2; Rare:186; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:99906563-99906711 | Rare:68 | ||||
| chr9:100098931-100099337 | Common:4; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352851-100353081 | Rare:83 | ||||
| chr9:101398511-101398910 | Common:1; Rare:141 |