| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98056798-98056857 | Rare:24 | ||||
| chr9:98119153-98119305 | Common:1; Rare:41 | ||||
| chr9:98255246-98255419 | Common:1; Rare:56 | ||||
| chr9:98255513-98255835 | Common:3; Rare:95 | ||||
| chr9:99104848-99105153 | Common:1; Rare:95 | ||||
| chr9:99221892-99222412 | Common:3; Rare:213; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:99821612-99822038 | Rare:123 | ||||
| chr9:99822044-99822107 | Rare:18 | ||||
| chr9:99822109-99822343 | Rare:57 | ||||
| chr9:100098920-100099324 | Common:3; Rare:114; Clinvar:2 | ||||
| chr9:100352775-100353103 | Rare:117 | ||||
| chr9:100427019-100427384 | Common:7; Rare:131 | ||||
| chr9:100429377-100429651 | Rare:42 | ||||
| chr9:101398585-101398983 | Common:1; Rare:117 | ||||
| chr9:101487028-101487278 | Common:3; Rare:61 |