| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151028280-151028490 | Rare:90 | ||||
| chr7:151057856-151058137 | Common:3; Rare:80 | ||||
| chr7:151062875-151063135 | Common:2; Rare:53 | ||||
| chr7:151080776-151080964 | Rare:55 | ||||
| chr7:151082980-151083150 | Rare:31 | ||||
| chr7:151083445-151083693 | Common:1; Rare:59 | ||||
| chr7:151232396-151232532 | Rare:46 | ||||
| chr7:151876904-151877663 | Common:4; Rare:183; Clinvar:7; Clinvar (benign):1 | ||||
| chr7:152025569-152025784 | Rare:88 | ||||
| chr7:152676089-152676316 | Common:2; Rare:105; Clinvar (benign):10 | ||||
| chr7:152759645-152759817 | Common:3; Rare:71 | ||||
| chr7:155003214-155003462 | Common:6; Rare:91 | ||||
| chr7:155644089-155644190 | Rare:39 | ||||
| chr7:155644308-155644919 | Common:6; Rare:194 | ||||
| chr7:156640548-156640794 | Common:2; Rare:115 |