| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:104207958-104208077 | Common:2; Rare:56 | ||||
| chr7:105013574-105013719 | Common:1; Rare:46 | ||||
| chr7:105014042-105014300 | Common:3; Rare:97 | ||||
| chr7:105014351-105014446 | Rare:32 | ||||
| chr7:105014452-105014485 | Rare:5 | ||||
| chr7:105107189-105107508 | Common:1; Rare:91 | ||||
| chr7:105532078-105532297 | Common:1; Rare:60 | ||||
| chr7:105876449-105876833 | Common:6; Rare:110 | ||||
| chr7:106112204-106112558 | Common:3; Rare:126 | ||||
| chr7:106284531-106284804 | Common:4; Rare:79 | ||||
| chr7:106284873-106285259 | Common:2; Rare:153 | ||||
| chr7:106285539-106285616 | Rare:21 | ||||
| chr7:107563840-107564047 | Common:2; Rare:119; Clinvar:2; Clinvar (benign):6 | ||||
| chr7:107564334-107564413 | Common:1; Rare:13; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:107580136-107580312 | Common:2; Rare:65 |