| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:23068988-23069242 | Common:1; Rare:100 | ||||
| chr8:23246269-23246672 | Common:5; Rare:122 | ||||
| chr8:23246730-23247080 | Rare:96 | ||||
| chr8:23404114-23404268 | Common:2; Rare:39 | ||||
| chr8:23457080-23457370 | Common:4; Rare:55 | ||||
| chr8:23457597-23457887 | Common:5; Rare:96 | ||||
| chr8:23528693-23529070 | Rare:124 | ||||
| chr8:24912910-24913190 | Common:2; Rare:52 | ||||
| chr8:24913591-24913775 | Rare:52 | ||||
| chr8:24913855-24914734 | Rare:417; Clinvar:6 | ||||
| chr8:24956033-24956171 | Rare:47; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr8:24956173-24956500 | Rare:107; Clinvar:12; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr8:24956596-24956803 | Common:3; Rare:46 | ||||
| chr8:24957213-24957613 | Common:9; Rare:96 | ||||
| chr8:25184505-25184804 | Common:1; Rare:96 |