| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105013538-105013719 | Common:1; Rare:61 | ||||
| chr7:105014034-105014341 | Common:3; Rare:109 | ||||
| chr7:105101191-105101523 | Common:4; Rare:64 | ||||
| chr7:105532078-105532279 | Common:1; Rare:55 | ||||
| chr7:105876470-105876844 | Common:6; Rare:109 | ||||
| chr7:105877354-105877564 | Common:3; Rare:31 | ||||
| chr7:106284885-106285476 | Common:6; Rare:215 | ||||
| chr7:106285539-106285569 | Rare:9 | ||||
| chr7:106661152-106661324 | Common:1; Rare:28 | ||||
| chr7:107168817-107169014 | Rare:66 | ||||
| chr7:107563846-107564021 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:107564327-107564358 | Rare:6; Clinvar:2 | ||||
| chr7:107580147-107580284 | Common:2; Rare:54 | ||||
| chr7:107743588-107743852 | Common:4; Rare:103 | ||||
| chr7:107743986-107744173 | Common:1; Rare:55 |