| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128476622-128476768 | Common:2; Rare:48 | ||||
| chr7:128739155-128739425 | Common:1; Rare:73 | ||||
| chr7:129054884-129055231 | Common:2; Rare:66 | ||||
| chr7:129611616-129611813 | Common:1; Rare:61 | ||||
| chr7:130051362-130051447 | Rare:32 | ||||
| chr7:130070291-130070542 | Common:2; Rare:61 | ||||
| chr7:131327704-131327901 | Rare:66 | ||||
| chr7:134646566-134646873 | Common:6; Rare:92 | ||||
| chr7:134986383-134986556 | Common:4; Rare:66 | ||||
| chr7:135147945-135148116 | Rare:38 | ||||
| chr7:135170645-135170816 | Common:2; Rare:66 | ||||
| chr7:139359684-139359988 | Common:3; Rare:121 | ||||
| chr7:141551307-141551428 | Rare:39; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738001-141738464 | Common:4; Rare:140 | ||||
| chr7:142854990-142855117 | Common:2; Rare:37 |