| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66682016-66682170 | Common:5; Rare:76 | ||||
| chr7:66921102-66921460 | Common:1; Rare:104 | ||||
| chr7:73308773-73308887 | Rare:47 | ||||
| chr7:73683396-73683624 | Common:3; Rare:95 | ||||
| chr7:73738723-73739012 | Common:1; Rare:96 | ||||
| chr7:74254352-74254520 | Rare:77 | ||||
| chr7:74289221-74289413 | Common:3; Rare:57 | ||||
| chr7:75994489-75994773 | Common:4; Rare:140 | ||||
| chr7:76047789-76048201 | Common:3; Rare:126 | ||||
| chr7:76302489-76303067 | Common:3; Rare:239; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:77696232-77696495 | Rare:115 | ||||
| chr7:77798455-77798974 | Common:1; Rare:130 | ||||
| chr7:79452858-79452992 | Common:1; Rare:31 | ||||
| chr7:79453803-79454130 | Common:2; Rare:77 | ||||
| chr7:84194920-84195115 | Common:4; Rare:47 |