| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:93916662-93917062 | Common:3; Rare:144; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:94262300-94262416 | Rare:37 | ||||
| chr8:94436907-94437036 | Rare:30 | ||||
| chr8:94553445-94553759 | Common:3; Rare:110 | ||||
| chr8:94719730-94719955 | Common:1; Rare:61 | ||||
| chr8:94895194-94895448 | Rare:74 | ||||
| chr8:94895696-94895849 | Common:2; Rare:42 | ||||
| chr8:95024951-95025166 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:96235510-96235652 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr8:96261579-96261957 | Common:5; Rare:122 | ||||
| chr8:96493748-96493823 | Rare:22 | ||||
| chr8:96645211-96645337 | Common:1; Rare:34 | ||||
| chr8:97277918-97278074 | Rare:50 | ||||
| chr8:98045333-98045663 | Common:3; Rare:98 | ||||
| chr8:98117114-98117366 | Common:4; Rare:82 |