| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:129054771-129054863 | Rare:32; Clinvar (benign):2 | ||||
| chr7:129054867-129055289 | Common:2; Rare:89 | ||||
| chr7:129434248-129434467 | Common:1; Rare:80 | ||||
| chr7:129611595-129611813 | Common:2; Rare:73 | ||||
| chr7:130051290-130051477 | Common:1; Rare:74 | ||||
| chr7:130070239-130070565 | Common:3; Rare:87 | ||||
| chr7:130205293-130205584 | Common:2; Rare:132 | ||||
| chr7:130440981-130441341 | Common:3; Rare:150; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:131109881-131110109 | Common:1; Rare:39 | ||||
| chr7:131327708-131327909 | Rare:66 | ||||
| chr7:133252874-133253123 | Rare:86 | ||||
| chr7:134316825-134317150 | Common:1; Rare:91 | ||||
| chr7:134459039-134459265 | Common:3; Rare:102 | ||||
| chr7:134646558-134646863 | Common:6; Rare:92 | ||||
| chr7:134779548-134779676 | Rare:25 |