| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100098955-100099314 | Common:3; Rare:102; Clinvar:2 | ||||
| chr9:100352841-100353069 | Rare:78 | ||||
| chr9:100429423-100429614 | Rare:31 | ||||
| chr9:101398584-101398887 | Common:1; Rare:100 | ||||
| chr9:104094533-104094603 | Rare:25 | ||||
| chr9:108934052-108934493 | Common:7; Rare:174; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110048523-110048777 | Common:2; Rare:89 | ||||
| chr9:110256410-110256720 | Common:4; Rare:108 | ||||
| chr9:112333516-112333944 | Rare:131 | ||||
| chr9:112379800-112380144 | Common:3; Rare:140 | ||||
| chr9:113188022-113188243 | Common:2; Rare:30 | ||||
| chr9:113221262-113221603 | Rare:108 | ||||
| chr9:113275376-113275734 | Common:5; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:113410652-113410840 | Common:2; Rare:63 | ||||
| chr9:114587554-114587877 | Common:3; Rare:128 |