| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44582129-44582532 | Common:1; Rare:158 | ||||
| chr7:44606440-44606641 | Common:1; Rare:66 | ||||
| chr7:44748307-44748591 | Common:2; Rare:69 | ||||
| chr7:44796390-44796769 | Common:3; Rare:150 | ||||
| chr7:45111665-45111818 | Common:1; Rare:58 | ||||
| chr7:47539594-47539802 | Common:2; Rare:42 | ||||
| chr7:47582075-47582194 | Common:1; Rare:43 | ||||
| chr7:48088532-48088747 | Common:2; Rare:44 | ||||
| chr7:48088871-48089331 | Common:7; Rare:123 | ||||
| chr7:48089441-48089576 | Common:2; Rare:34 | ||||
| chr7:50450311-50450447 | Common:1; Rare:56 | ||||
| chr7:55018910-55019240 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:55572312-55572574 | Common:1; Rare:102 | ||||
| chr7:55951780-55951940 | Rare:48 | ||||
| chr7:56051361-56051851 | Common:1; Rare:182; Clinvar:6; Clinvar (benign):1 |