| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94719761-94719955 | Common:1; Rare:53 | ||||
| chr8:94895199-94895322 | Rare:41 | ||||
| chr8:94895668-94895802 | Rare:43 | ||||
| chr8:94949351-94949544 | Common:1; Rare:59 | ||||
| chr8:95024937-95025159 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95269198-95269310 | Common:5; Rare:45; Clinvar:1 | ||||
| chr8:96235510-96235669 | Common:1; Rare:84; Clinvar (benign):2 | ||||
| chr8:96261557-96261974 | Common:6; Rare:140 | ||||
| chr8:96493728-96494330 | Common:4; Rare:190 | ||||
| chr8:96645211-96645401 | Common:1; Rare:52 | ||||
| chr8:97643869-97644223 | Common:8; Rare:88 | ||||
| chr8:97868933-97869140 | Common:1; Rare:43 | ||||
| chr8:98031992-98032309 | Common:4; Rare:61 | ||||
| chr8:98045327-98045660 | Common:3; Rare:101 | ||||
| chr8:98117108-98117333 | Common:4; Rare:78 |