| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105269008-105269297 | Rare:46 | ||||
| chr7:105389366-105389416 | Rare:17 | ||||
| chr7:105521939-105522404 | Common:8; Rare:138 | ||||
| chr7:105532047-105532244 | Common:3; Rare:49 | ||||
| chr7:105581459-105581566 | Rare:36 | ||||
| chr7:105876477-105876844 | Common:6; Rare:109 | ||||
| chr7:106112204-106112634 | Common:3; Rare:153 | ||||
| chr7:106284429-106285268 | Common:6; Rare:296 | ||||
| chr7:106285406-106285571 | Rare:45 | ||||
| chr7:106285684-106285856 | Common:1; Rare:29 | ||||
| chr7:106285878-106286186 | Common:1; Rare:67 | ||||
| chr7:107168720-107169021 | Rare:100 | ||||
| chr7:107469710-107470086 | Common:1; Rare:87 | ||||
| chr7:107563840-107564053 | Common:2; Rare:123; Clinvar:2; Clinvar (benign):6 | ||||
| chr7:107580145-107580294 | Common:2; Rare:61 |