| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906601-99906690 | Rare:46 | ||||
| chr9:100098966-100099307 | Common:3; Rare:96; Clinvar:1 | ||||
| chr9:100352831-100353089 | Rare:93 | ||||
| chr9:101398556-101398910 | Common:1; Rare:125 | ||||
| chr9:101533690-101533907 | Rare:68 | ||||
| chr9:104093985-104094346 | Common:3; Rare:88 | ||||
| chr9:104094522-104094603 | Common:1; Rare:26 | ||||
| chr9:104747617-104747767 | Rare:42 | ||||
| chr9:105558060-105558163 | Rare:32; Clinvar (benign):1 | ||||
| chr9:108934074-108934496 | Common:7; Rare:170; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110256418-110256720 | Common:4; Rare:106 | ||||
| chr9:111038673-111038816 | Common:4; Rare:34 | ||||
| chr9:111631180-111631503 | Common:1; Rare:96 | ||||
| chr9:111661487-111661673 | Common:3; Rare:55 | ||||
| chr9:112379793-112380140 | Common:4; Rare:137 |