| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97922423-97922585 | Common:4; Rare:85 | ||||
| chr9:97983116-97983451 | Common:1; Rare:126 | ||||
| chr9:98056409-98056791 | Common:6; Rare:118 | ||||
| chr9:98192630-98192811 | Common:5; Rare:51 | ||||
| chr9:99221898-99222355 | Common:2; Rare:181; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:99906574-99906717 | Rare:67 | ||||
| chr9:100098970-100099314 | Common:3; Rare:96; Clinvar:2 | ||||
| chr9:100352831-100353092 | Rare:96 | ||||
| chr9:101398580-101398887 | Common:1; Rare:104 | ||||
| chr9:101487097-101487190 | Common:2; Rare:21 | ||||
| chr9:101533748-101533914 | Rare:53 | ||||
| chr9:104093973-104094321 | Common:3; Rare:87 | ||||
| chr9:104747559-104747802 | Common:1; Rare:73 | ||||
| chr9:104928135-104928302 | Common:3; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:105447897-105448135 | Common:5; Rare:86 |