| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75994502-75994772 | Common:4; Rare:134 | ||||
| chr7:76047799-76048238 | Common:3; Rare:143 | ||||
| chr7:76302520-76303081 | Common:3; Rare:234; Clinvar:18; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303365-76303641 | Common:4; Rare:102 | ||||
| chr7:76303659-76303865 | Common:1; Rare:93; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:77122312-77122638 | Common:2; Rare:68 | ||||
| chr7:77199784-77199845 | Rare:19 | ||||
| chr7:77199852-77199942 | Rare:15 | ||||
| chr7:77537969-77538106 | Common:3; Rare:52 | ||||
| chr7:77696133-77696527 | Common:1; Rare:162 | ||||
| chr7:77696756-77696960 | Rare:88 | ||||
| chr7:77798344-77798956 | Common:1; Rare:146 | ||||
| chr7:79453598-79453689 | Rare:27 | ||||
| chr7:79453809-79454117 | Common:2; Rare:73 | ||||
| chr7:87152300-87152675 | Common:2; Rare:113 |