| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:102748692-102749210 | Common:3; Rare:134 | ||||
| chr7:102912886-102913098 | Common:3; Rare:50 | ||||
| chr7:103149055-103149371 | Common:4; Rare:90 | ||||
| chr7:103344696-103344869 | Common:1; Rare:56 | ||||
| chr7:104207956-104208123 | Common:3; Rare:77 | ||||
| chr7:105014062-105014291 | Common:2; Rare:87 | ||||
| chr7:105268981-105269129 | Rare:24 | ||||
| chr7:105532055-105532246 | Common:3; Rare:48 | ||||
| chr7:105581452-105581550 | Rare:38 | ||||
| chr7:105876481-105876844 | Common:6; Rare:108 | ||||
| chr7:106112478-106112711 | Common:1; Rare:94 | ||||
| chr7:106284871-106285276 | Common:2; Rare:163 | ||||
| chr7:106285539-106285665 | Rare:30 | ||||
| chr7:107469803-107470233 | Common:1; Rare:97 | ||||
| chr7:107563879-107563997 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):2 |