| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:88220017-88220163 | Rare:68 | ||||
| chr7:90154252-90154502 | Rare:60 | ||||
| chr7:90211573-90211934 | Common:4; Rare:111 | ||||
| chr7:90245083-90245221 | Rare:40 | ||||
| chr7:90346607-90346749 | Common:3; Rare:67 | ||||
| chr7:91880668-91880771 | Common:1; Rare:29 | ||||
| chr7:92134361-92134556 | Rare:56 | ||||
| chr7:92134711-92134923 | Common:3; Rare:62 | ||||
| chr7:92245849-92246347 | Common:6; Rare:135; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528306-92528816 | Common:3; Rare:152; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833925-92834030 | Rare:25 | ||||
| chr7:93232176-93232389 | Common:2; Rare:43 | ||||
| chr7:93591198-93591419 | Common:1; Rare:70 | ||||
| chr7:93890756-93890840 | Common:1; Rare:23 | ||||
| chr7:93922038-93922059 | Rare:4 |