| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:93794697-93794922 | Common:1; Rare:29 | ||||
| chr8:93916637-93917055 | Common:4; Rare:150; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:94436926-94437055 | Rare:30 | ||||
| chr8:94553440-94553769 | Common:3; Rare:117 | ||||
| chr8:94719771-94720147 | Common:4; Rare:111 | ||||
| chr8:94895688-94895822 | Common:1; Rare:37 | ||||
| chr8:94949357-94949553 | Common:1; Rare:59 | ||||
| chr8:95024754-95025184 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95133597-95133928 | Common:3; Rare:106 | ||||
| chr8:96235483-96235696 | Common:1; Rare:117; Clinvar (benign):3 | ||||
| chr8:96261528-96261981 | Common:6; Rare:154 | ||||
| chr8:96493795-96493830 | Rare:10 | ||||
| chr8:96494123-96494330 | Common:1; Rare:71 | ||||
| chr8:97277897-97278058 | Rare:53 | ||||
| chr8:97643844-97644360 | Common:9; Rare:134 |