| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87152317-87152474 | Common:1; Rare:51 | ||||
| chr7:87220526-87220682 | Common:1; Rare:45 | ||||
| chr7:87345443-87345706 | Common:4; Rare:86 | ||||
| chr7:87876224-87876685 | Common:3; Rare:196 | ||||
| chr7:90346596-90346752 | Common:4; Rare:70 | ||||
| chr7:90709768-90709823 | Common:1; Rare:12 | ||||
| chr7:90710016-90710161 | Rare:19 | ||||
| chr7:90726141-90726294 | Common:1; Rare:21 | ||||
| chr7:91880657-91880801 | Common:1; Rare:42 | ||||
| chr7:91940749-91940979 | Common:4; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:92134405-92134556 | Rare:44 | ||||
| chr7:92134717-92134923 | Common:3; Rare:61 | ||||
| chr7:92245894-92245991 | Rare:28; Clinvar:3 | ||||
| chr7:92528345-92528829 | Common:4; Rare:152; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93117951-93118106 | Rare:27 |