| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108933929-108934203 | Common:3; Rare:98; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:108934270-108934610 | Common:7; Rare:146; Clinvar (benign):1 | ||||
| chr9:109119524-109119672 | Common:3; Rare:70 | ||||
| chr9:109119909-109120230 | Common:14; Rare:105 | ||||
| chr9:109779990-109780460 | Common:3; Rare:122 | ||||
| chr9:110048466-110048718 | Common:1; Rare:68 | ||||
| chr9:110125345-110125534 | Rare:36 | ||||
| chr9:110256436-110256728 | Common:5; Rare:106 | ||||
| chr9:110579149-110579683 | Common:4; Rare:294 | ||||
| chr9:110579727-110579968 | Common:2; Rare:68 | ||||
| chr9:111037326-111038229 | Common:1; Rare:198 | ||||
| chr9:111038380-111038990 | Common:10; Rare:138 | ||||
| chr9:111483879-111484165 | Rare:114 | ||||
| chr9:111484316-111484533 | Rare:126 | ||||
| chr9:111524991-111525250 | Common:6; Rare:82 |