| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94598926-94599018 | Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:94656100-94656380 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95396357-95396532 | Common:2; Rare:75 | ||||
| chr7:95596155-95596229 | Rare:27 | ||||
| chr7:95596441-95596722 | Common:5; Rare:50 | ||||
| chr7:96321998-96322171 | Rare:86; Clinvar:4 | ||||
| chr7:97117457-97117759 | Common:2; Rare:131 | ||||
| chr7:97872401-97872592 | Common:2; Rare:60 | ||||
| chr7:98106553-98107004 | Common:2; Rare:105 | ||||
| chr7:98107135-98107241 | Common:1; Rare:34 | ||||
| chr7:98252124-98252406 | Common:2; Rare:67 | ||||
| chr7:98282125-98282441 | Common:2; Rare:110 | ||||
| chr7:99325794-99326001 | Common:1; Rare:82 | ||||
| chr7:99390860-99390928 | Common:1; Rare:16 | ||||
| chr7:99390940-99391239 | Rare:105 |