| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44999603-44999777 | Common:3; Rare:63 | ||||
| chr7:44999984-45000358 | Common:1; Rare:87; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:45111651-45111822 | Common:1; Rare:68 | ||||
| chr7:48089023-48089286 | Common:3; Rare:69 | ||||
| chr7:50450322-50450445 | Common:1; Rare:50 | ||||
| chr7:55018910-55019112 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:55019314-55019360 | Rare:15 | ||||
| chr7:55365196-55365369 | Common:1; Rare:46 | ||||
| chr7:55365870-55366085 | Rare:87 | ||||
| chr7:55366284-55366402 | Common:1; Rare:44 | ||||
| chr7:55572444-55572665 | Common:2; Rare:78 | ||||
| chr7:55951739-55951964 | Rare:65 | ||||
| chr7:56051351-56051985 | Common:1; Rare:218; Clinvar:6; Clinvar (benign):1 | ||||
| chr7:56063846-56064320 | Common:2; Rare:188 | ||||
| chr7:56064336-56064375 | Rare:20 |