| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91264202-91264450 | Common:1; Rare:63 | ||||
| chr7:91880661-91880823 | Common:2; Rare:45 | ||||
| chr7:92097870-92098207 | Common:3; Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134424-92134556 | Rare:37 | ||||
| chr7:92134786-92134852 | Common:2; Rare:16 | ||||
| chr7:92245865-92245979 | Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528358-92528808 | Common:3; Rare:134; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833926-92834080 | Rare:37 | ||||
| chr7:93232201-93232407 | Common:2; Rare:41 | ||||
| chr7:93890626-93890914 | Common:4; Rare:83 | ||||
| chr7:94656094-94656383 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95396358-95396528 | Common:2; Rare:70 | ||||
| chr7:95434908-95435102 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr7:95589649-95589985 | Common:2; Rare:61 | ||||
| chr7:95596162-95596199 | Rare:10 |