| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:127651820-127652235 | Common:3; Rare:122 | ||||
| chr7:128400162-128400383 | Rare:70; Clinvar:3 | ||||
| chr7:128455663-128455924 | Common:3; Rare:132 | ||||
| chr7:128476645-128476840 | Common:1; Rare:75 | ||||
| chr7:128739159-128739431 | Common:1; Rare:71 | ||||
| chr7:128830171-128830421 | Common:2; Rare:64 | ||||
| chr7:128830912-128830989 | Rare:20; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:128910686-128910894 | Common:2; Rare:57 | ||||
| chr7:129054884-129055219 | Common:1; Rare:65 | ||||
| chr7:129611616-129611781 | Common:1; Rare:53 | ||||
| chr7:130070302-130070565 | Common:1; Rare:68 | ||||
| chr7:130205391-130205525 | Rare:61 | ||||
| chr7:130492026-130492335 | Common:1; Rare:81 | ||||
| chr7:131109922-131110029 | Rare:17 | ||||
| chr7:131327711-131327924 | Rare:75 |