| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128739152-128739427 | Common:2; Rare:73 | ||||
| chr7:129054873-129055239 | Common:2; Rare:68 | ||||
| chr7:129434248-129434460 | Common:1; Rare:78 | ||||
| chr7:129611616-129611803 | Common:1; Rare:59 | ||||
| chr7:130051342-130051437 | Rare:40 | ||||
| chr7:130070291-130070572 | Common:2; Rare:74 | ||||
| chr7:130205373-130205526 | Rare:73 | ||||
| chr7:130292882-130293202 | Common:2; Rare:57 | ||||
| chr7:130440977-130441306 | Common:3; Rare:138; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:131109876-131110105 | Common:1; Rare:40 | ||||
| chr7:131327697-131327902 | Rare:66 | ||||
| chr7:134316849-134317077 | Rare:64 | ||||
| chr7:134459043-134459291 | Common:4; Rare:111 | ||||
| chr7:134646553-134646904 | Common:8; Rare:115 | ||||
| chr7:135148035-135148087 | Rare:13 |