| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94004233-94004495 | Rare:74 | ||||
| chr7:94425779-94426034 | Rare:80; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:94656100-94656379 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95396363-95396508 | Common:2; Rare:60 | ||||
| chr7:95837233-95837618 | Common:10; Rare:42 | ||||
| chr7:96322031-96322182 | Rare:70; Clinvar:4 | ||||
| chr7:96709778-96709923 | Rare:48 | ||||
| chr7:97117449-97117759 | Common:2; Rare:132 | ||||
| chr7:98252216-98252372 | Rare:37 | ||||
| chr7:98878437-98878601 | Rare:56 | ||||
| chr7:99325707-99325968 | Common:1; Rare:108 | ||||
| chr7:99408537-99409037 | Common:3; Rare:143 | ||||
| chr7:99438721-99438996 | Common:1; Rare:88 | ||||
| chr7:99439264-99439438 | Common:2; Rare:39 | ||||
| chr7:99466120-99466258 | Rare:50 |