| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105014459-105014713 | Rare:46 | ||||
| chr7:105532098-105532256 | Common:1; Rare:40 | ||||
| chr7:105876470-105876900 | Common:7; Rare:125 | ||||
| chr7:105877163-105877252 | Rare:17 | ||||
| chr7:105877354-105877564 | Common:3; Rare:31 | ||||
| chr7:106112274-106112509 | Common:2; Rare:74 | ||||
| chr7:106284885-106285262 | Common:2; Rare:152 | ||||
| chr7:106285539-106285556 | Rare:6 | ||||
| chr7:106661150-106661411 | Common:1; Rare:42 | ||||
| chr7:107563848-107564037 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107564332-107564399 | Common:1; Rare:13; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:107580174-107580294 | Common:2; Rare:44 | ||||
| chr7:107744042-107744171 | Rare:42 | ||||
| chr7:107929109-107929711 | Common:3; Rare:169; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:108003110-108003243 | Rare:39 |