| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100874955-100875223 | Common:2; Rare:92 | ||||
| chr7:101154323-101154503 | Common:1; Rare:64 | ||||
| chr7:101217850-101218198 | Common:4; Rare:111 | ||||
| chr7:101245053-101245191 | Common:1; Rare:47 | ||||
| chr7:101252282-101252538 | Common:1; Rare:54 | ||||
| chr7:101321711-101321918 | Common:3; Rare:73 | ||||
| chr7:102748670-102748974 | Common:3; Rare:60 | ||||
| chr7:103344716-103344921 | Common:1; Rare:57 | ||||
| chr7:104207954-104208086 | Common:2; Rare:65 | ||||
| chr7:105014097-105014255 | Common:1; Rare:67 | ||||
| chr7:105532071-105532231 | Rare:43 | ||||
| chr7:105876481-105876844 | Common:6; Rare:108 | ||||
| chr7:106284978-106285222 | Common:2; Rare:87 | ||||
| chr7:107563862-107564021 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:107580162-107580294 | Common:2; Rare:54 |