| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101245024-101245190 | Common:1; Rare:69 | ||||
| chr7:102464848-102465014 | Rare:68 | ||||
| chr7:105013564-105013687 | Common:1; Rare:42 | ||||
| chr7:105014087-105014261 | Common:1; Rare:72 | ||||
| chr7:105532086-105532240 | Common:1; Rare:41 | ||||
| chr7:105876481-105876829 | Common:6; Rare:104 | ||||
| chr7:106661138-106661270 | Common:1; Rare:21 | ||||
| chr7:107168728-107169015 | Rare:97 | ||||
| chr7:107563861-107564021 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:107580181-107580312 | Common:2; Rare:43 | ||||
| chr7:107744053-107744171 | Rare:37 | ||||
| chr7:108569563-108570077 | Common:4; Rare:181 | ||||
| chr7:112206420-112206751 | Common:1; Rare:120 | ||||
| chr7:112939714-112940071 | Common:4; Rare:124 | ||||
| chr7:116210350-116210682 | Common:4; Rare:82 |