| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107169693-107170109 | Common:4; Rare:121 | ||||
| chr7:107563861-107564071 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:107564336-107564622 | Common:2; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:107580123-107580312 | Common:2; Rare:69 | ||||
| chr7:107693164-107693298 | Common:1; Rare:30 | ||||
| chr7:107743579-107743865 | Common:5; Rare:112 | ||||
| chr7:107743994-107744196 | Common:1; Rare:67 | ||||
| chr7:107891411-107891440 | Rare:7 | ||||
| chr7:107929601-107929703 | Rare:24 | ||||
| chr7:108526034-108526475 | Common:5; Rare:130 | ||||
| chr7:108569460-108570013 | Common:4; Rare:195 | ||||
| chr7:111392813-111393532 | Rare:145 | ||||
| chr7:111562463-111562611 | Rare:63 | ||||
| chr7:112206291-112206789 | Common:2; Rare:169 | ||||
| chr7:112450287-112450470 | Common:4; Rare:60 |