| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:50792872-50792998 | Common:2; Rare:40 | ||||
| chr7:51316771-51317011 | Common:5; Rare:84 | ||||
| chr7:55365280-55365367 | Rare:22 | ||||
| chr7:55365512-55365533 | Rare:6 | ||||
| chr7:55365875-55366076 | Rare:81 | ||||
| chr7:55366234-55366413 | Common:1; Rare:81 | ||||
| chr7:55572443-55572765 | Common:3; Rare:100 | ||||
| chr7:55887435-55887544 | Rare:30 | ||||
| chr7:55951739-55951942 | Rare:59 | ||||
| chr7:55964404-55964682 | Common:1; Rare:96 | ||||
| chr7:55964842-55965010 | Common:1; Rare:43 | ||||
| chr7:56034084-56034272 | Rare:54 | ||||
| chr7:56051374-56051986 | Common:1; Rare:211; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56063985-56064360 | Common:2; Rare:182 | ||||
| chr7:56106444-56106671 | Common:6; Rare:71 |