| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87876349-87876541 | Rare:83 | ||||
| chr7:90595846-90596034 | Common:6; Rare:63 | ||||
| chr7:91880662-91880813 | Common:1; Rare:43 | ||||
| chr7:92245890-92245994 | Rare:30; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528451-92528811 | Common:3; Rare:112; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:93921983-93922112 | Common:3; Rare:34 | ||||
| chr7:94004289-94004476 | Rare:51 | ||||
| chr7:94394547-94395096 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:94656092-94656381 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:97117505-97117707 | Rare:71 | ||||
| chr7:98252151-98252364 | Common:1; Rare:51 | ||||
| chr7:99325801-99325983 | Common:1; Rare:71 | ||||
| chr7:99408552-99408665 | Common:2; Rare:36 | ||||
| chr7:99408780-99409040 | Common:1; Rare:80 | ||||
| chr7:99438749-99439029 | Common:2; Rare:77 |