| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94262130-94262570 | Rare:95 | ||||
| chr8:94436429-94436662 | Common:1; Rare:45 | ||||
| chr8:94436922-94437119 | Rare:40 | ||||
| chr8:94474944-94475174 | Common:4; Rare:69 | ||||
| chr8:94553432-94553805 | Common:3; Rare:134 | ||||
| chr8:94719692-94719992 | Common:1; Rare:91 | ||||
| chr8:94823145-94823352 | Common:2; Rare:73 | ||||
| chr8:94893449-94893849 | Common:2; Rare:73 | ||||
| chr8:94895643-94895802 | Rare:46 | ||||
| chr8:94896560-94896910 | Common:7; Rare:78 | ||||
| chr8:94949280-94949611 | Common:3; Rare:89 | ||||
| chr8:95024873-95025187 | Common:2; Rare:119; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95133550-95133900 | Common:2; Rare:116 | ||||
| chr8:95133947-95134471 | Common:4; Rare:225 | ||||
| chr8:95268683-95268898 | Common:10; Rare:62 |