| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98192630-98192880 | Common:6; Rare:68 | ||||
| chr9:99221940-99222357 | Common:2; Rare:155; Clinvar:2 | ||||
| chr9:99906575-99906694 | Rare:61 | ||||
| chr9:100098937-100099314 | Common:3; Rare:104; Clinvar:2 | ||||
| chr9:100352858-100353089 | Rare:83 | ||||
| chr9:101028628-101029053 | Common:4; Rare:128 | ||||
| chr9:101398556-101398910 | Common:1; Rare:125 | ||||
| chr9:101487092-101487190 | Common:2; Rare:22 | ||||
| chr9:101533700-101533894 | Rare:55 | ||||
| chr9:104093977-104094346 | Common:3; Rare:92 | ||||
| chr9:104747634-104747802 | Common:1; Rare:53 | ||||
| chr9:104928147-104928443 | Common:5; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:105447966-105448153 | Common:2; Rare:70 | ||||
| chr9:105558033-105558170 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862953-106863180 | Rare:75 |