| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128791323-128791493 | Rare:43 | ||||
| chr7:129054873-129055267 | Common:2; Rare:80 | ||||
| chr7:129434236-129434460 | Common:1; Rare:83 | ||||
| chr7:129611616-129611772 | Common:1; Rare:49 | ||||
| chr7:130051340-130051461 | Rare:45 | ||||
| chr7:130070284-130070578 | Common:2; Rare:77 | ||||
| chr7:130205293-130205584 | Common:2; Rare:132 | ||||
| chr7:130345112-130345274 | Common:3; Rare:26 | ||||
| chr7:130440981-130441293 | Common:3; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:130490949-130491277 | Common:1; Rare:70 | ||||
| chr7:131327810-131327905 | Rare:40 | ||||
| chr7:133252892-133253104 | Rare:72 | ||||
| chr7:134316834-134317175 | Common:2; Rare:98 | ||||
| chr7:134646577-134646864 | Common:6; Rare:85 | ||||
| chr7:134891364-134891643 | Common:3; Rare:80 |