| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94719745-94720014 | Common:1; Rare:81 | ||||
| chr8:94895194-94895360 | Rare:53 | ||||
| chr8:94895622-94895860 | Common:3; Rare:65 | ||||
| chr8:95024937-95025203 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95133597-95133964 | Common:3; Rare:117 | ||||
| chr8:95269190-95269311 | Common:5; Rare:49; Clinvar:1 | ||||
| chr8:95269376-95269435 | Common:3; Rare:14 | ||||
| chr8:96235510-96235661 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr8:96261549-96261998 | Common:6; Rare:151 | ||||
| chr8:96493549-96493852 | Rare:94 | ||||
| chr8:96645225-96645375 | Common:1; Rare:39 | ||||
| chr8:97643856-97644213 | Common:8; Rare:85 | ||||
| chr8:97644258-97644360 | Rare:30 | ||||
| chr8:97644647-97644881 | Common:1; Rare:79 | ||||
| chr8:97775724-97776015 | Common:4; Rare:148; Clinvar (benign):1 |