| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128830193-128830460 | Common:4; Rare:75 | ||||
| chr7:128830582-128830771 | Rare:70; Clinvar:6; Clinvar (benign):3 | ||||
| chr7:129054873-129055240 | Common:2; Rare:69 | ||||
| chr7:129434248-129434470 | Common:1; Rare:81 | ||||
| chr7:129611595-129611798 | Common:2; Rare:70 | ||||
| chr7:129951276-129951650 | Common:3; Rare:77 | ||||
| chr7:129951908-129952129 | Common:2; Rare:48 | ||||
| chr7:130051342-130051425 | Rare:34 | ||||
| chr7:130070257-130070573 | Common:2; Rare:85 | ||||
| chr7:130205377-130205574 | Rare:85 | ||||
| chr7:130380263-130380432 | Rare:26 | ||||
| chr7:130440981-130441318 | Common:3; Rare:141; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:131110026-131110083 | Common:1; Rare:7 | ||||
| chr7:131327658-131327909 | Rare:73 | ||||
| chr7:134316825-134317175 | Common:2; Rare:100 |