| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134646582-134646907 | Common:7; Rare:104 | ||||
| chr7:135170669-135170907 | Common:3; Rare:84 | ||||
| chr7:135510089-135510312 | Common:2; Rare:43 | ||||
| chr7:135662383-135662511 | Common:3; Rare:56 | ||||
| chr7:139341166-139341350 | Rare:40 | ||||
| chr7:139359692-139359974 | Common:2; Rare:113 | ||||
| chr7:141738031-141738464 | Common:4; Rare:133 | ||||
| chr7:151057856-151058253 | Common:4; Rare:108 | ||||
| chr7:151080793-151080962 | Rare:51 | ||||
| chr7:155644377-155644697 | Common:2; Rare:104 | ||||
| chr7:157336790-157337064 | Common:2; Rare:125; Clinvar:1 | ||||
| chr7:158856423-158856632 | Common:5; Rare:73 | ||||
| chr8:232223-232377 | Common:2; Rare:61 | ||||
| chr8:6406533-6406647 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:6708530-6708671 | Common:1; Rare:59 |