| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128405913-128406135 | Common:2; Rare:79 | ||||
| chr7:128409920-128410173 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455663-128455919 | Common:3; Rare:129 | ||||
| chr7:128739176-128739427 | Common:1; Rare:64 | ||||
| chr7:128791323-128791490 | Rare:43 | ||||
| chr7:128830134-128830449 | Common:4; Rare:80 | ||||
| chr7:128830574-128830764 | Rare:69; Clinvar:6; Clinvar (benign):3 | ||||
| chr7:128830905-128830988 | Rare:21; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:129054804-129055231 | Common:2; Rare:91; Clinvar (benign):1 | ||||
| chr7:129611600-129611783 | Common:2; Rare:61 | ||||
| chr7:130051347-130051440 | Rare:37 | ||||
| chr7:130205385-130205711 | Rare:105 | ||||
| chr7:131109818-131110136 | Common:1; Rare:60 | ||||
| chr7:131327697-131327909 | Rare:66 | ||||
| chr7:134646566-134646856 | Common:6; Rare:83 |