| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106285830-106285875 | Common:1; Rare:4 | ||||
| chr7:106285878-106285927 | Common:1; Rare:15 | ||||
| chr7:106661020-106661305 | Common:2; Rare:70 | ||||
| chr7:107168509-107168624 | Common:1; Rare:33 | ||||
| chr7:107168720-107169027 | Rare:104 | ||||
| chr7:107563879-107564028 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107564330-107564347 | Rare:2; Clinvar:1 | ||||
| chr7:107580162-107580297 | Common:2; Rare:55 | ||||
| chr7:107743589-107743865 | Common:5; Rare:107 | ||||
| chr7:107744042-107744190 | Rare:51 | ||||
| chr7:107929412-107929770 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:108003088-108003469 | Common:4; Rare:115 | ||||
| chr7:108526020-108526475 | Common:5; Rare:133 | ||||
| chr7:108569576-108570056 | Common:2; Rare:170 | ||||
| chr7:111561900-111562139 | Rare:64 |