| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:116672266-116672454 | Common:1; Rare:45; Clinvar:2 | ||||
| chr7:116953254-116953543 | Common:2; Rare:73 | ||||
| chr7:118183965-118184226 | Common:2; Rare:100 | ||||
| chr7:120950578-120950833 | Common:2; Rare:80 | ||||
| chr7:121328766-121329036 | Rare:79 | ||||
| chr7:122144203-122144415 | Common:1; Rare:46 | ||||
| chr7:123748730-123748819 | Rare:32 | ||||
| chr7:123748822-123749264 | Common:3; Rare:155 | ||||
| chr7:123749556-123749578 | Rare:3 | ||||
| chr7:124929802-124929894 | Common:2; Rare:27 | ||||
| chr7:127392071-127392328 | Rare:100 | ||||
| chr7:127588103-127588496 | Common:1; Rare:136 | ||||
| chr7:127651827-127652266 | Common:3; Rare:129 | ||||
| chr7:128405943-128406141 | Common:2; Rare:70 | ||||
| chr7:128409932-128410044 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 |