| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100091386-100091672 | Rare:103 | ||||
| chr7:100113729-100113921 | Common:4; Rare:95; Clinvar (pathogenic):1 | ||||
| chr7:100335870-100336189 | Common:1; Rare:99 | ||||
| chr7:100345984-100346140 | Rare:22 | ||||
| chr7:100856002-100856012 | |||||
| chr7:102822455-102822588 | Common:1; Rare:17 | ||||
| chr7:103321771-103322011 | Common:1; Rare:60 | ||||
| chr7:103355511-103355743 | Rare:40 | ||||
| chr7:105013025-105013217 | Common:1; Rare:67 | ||||
| chr7:105105191-105105690 | Common:1; Rare:113 | ||||
| chr7:107195092-107195236 | Rare:30 | ||||
| chr7:107929148-107929318 | Common:1; Rare:47 | ||||
| chr7:107945552-107945634 | Rare:18 | ||||
| chr7:108059477-108059554 | Rare:14 | ||||
| chr7:108061765-108061910 | Rare:21 |