| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94719761-94719973 | Common:1; Rare:64 | ||||
| chr8:94895679-94895851 | Common:3; Rare:55 | ||||
| chr8:94949339-94949567 | Common:2; Rare:69 | ||||
| chr8:95024895-95025184 | Common:2; Rare:111; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:96235510-96235652 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr8:96261566-96261981 | Common:6; Rare:137 | ||||
| chr8:96493620-96494330 | Common:4; Rare:220 | ||||
| chr8:96645144-96645397 | Common:2; Rare:72 | ||||
| chr8:97644467-97644768 | Common:2; Rare:96 | ||||
| chr8:97868981-97869211 | Common:2; Rare:46 | ||||
| chr8:98031976-98032317 | Common:4; Rare:64 | ||||
| chr8:98045336-98045676 | Common:4; Rare:100 | ||||
| chr8:98117098-98117317 | Common:2; Rare:79 | ||||
| chr8:99013007-99013368 | Rare:76; Clinvar:1 | ||||
| chr8:100309365-100309489 | Rare:29 |