| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105507902-105508900 | Common:14; Rare:314; Clinvar (pathogenic):2 | ||||
| chr7:105522168-105522337 | Common:4; Rare:114 | ||||
| chr7:105532054-105532285 | Common:4; Rare:118 | ||||
| chr7:105581336-105581736 | Rare:182 | ||||
| chr7:105876473-105876975 | Common:15; Rare:260 | ||||
| chr7:105877353-105877551 | Common:2; Rare:30 | ||||
| chr7:106112191-106112494 | Common:6; Rare:153 | ||||
| chr7:106284911-106285417 | Common:9; Rare:332 | ||||
| chr7:107168392-107169165 | Common:4; Rare:472 | ||||
| chr7:107169510-107169950 | Common:8; Rare:249 | ||||
| chr7:107563831-107564032 | Common:4; Rare:207; Clinvar:2; Clinvar (benign):9 | ||||
| chr7:107564460-107564690 | Common:1; Rare:63; Clinvar:1 | ||||
| chr7:107580079-107580296 | Common:2; Rare:78 | ||||
| chr7:107743460-107743930 | Common:10; Rare:265 | ||||
| chr7:107744018-107744205 | Rare:101 |