| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:71131475-71131732 | Common:5; Rare:86 | ||||
| chr7:72828138-72828458 | Common:1; Rare:93 | ||||
| chr7:73308780-73308879 | Rare:44 | ||||
| chr7:73557089-73557361 | Common:1; Rare:98 | ||||
| chr7:73557585-73557733 | Common:2; Rare:54 | ||||
| chr7:73683396-73683794 | Common:4; Rare:175 | ||||
| chr7:73738669-73739033 | Common:1; Rare:126 | ||||
| chr7:73739129-73739252 | Rare:25 | ||||
| chr7:73739254-73739309 | Rare:13 | ||||
| chr7:73739313-73739356 | Rare:10 | ||||
| chr7:73769465-73769996 | Common:2; Rare:161 | ||||
| chr7:73770268-73770558 | Rare:56 | ||||
| chr7:73842505-73842693 | Common:6; Rare:27 | ||||
| chr7:74028032-74028261 | Common:1; Rare:82; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:74045158-74045266 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):2 |