| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100874890-100875202 | Common:1; Rare:113 | ||||
| chr7:101217850-101218198 | Common:4; Rare:111 | ||||
| chr7:101245055-101245173 | Common:1; Rare:41 | ||||
| chr7:101321733-101321880 | Common:3; Rare:50 | ||||
| chr7:101815649-101816023 | Common:1; Rare:101 | ||||
| chr7:102464829-102465014 | Common:1; Rare:75 | ||||
| chr7:104207989-104208099 | Common:1; Rare:41 | ||||
| chr7:105014097-105014210 | Common:1; Rare:49 | ||||
| chr7:105532055-105532218 | Common:2; Rare:42 | ||||
| chr7:105876481-105876812 | Common:6; Rare:98 | ||||
| chr7:106284978-106285208 | Common:2; Rare:81 | ||||
| chr7:107563897-107563996 | Common:2; Rare:59; Clinvar (benign):2 | ||||
| chr7:107580126-107580294 | Common:2; Rare:67 | ||||
| chr7:107744021-107744171 | Rare:45 | ||||
| chr7:108569615-108569959 | Common:1; Rare:118 |