| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:813358-813507 | Rare:53 | ||||
| chr7:1532804-1532981 | Common:1; Rare:43 | ||||
| chr7:5397228-5397528 | Rare:84 | ||||
| chr7:5426675-5426858 | Common:2; Rare:44 | ||||
| chr7:5427797-5428152 | Common:2; Rare:154 | ||||
| chr7:5695490-5695705 | Common:2; Rare:49 | ||||
| chr7:7183165-7183280 | Common:1; Rare:38 | ||||
| chr7:16989967-16990240 | Common:2; Rare:57 | ||||
| chr7:17099557-17099758 | Common:3; Rare:51 | ||||
| chr7:24979303-24979558 | Common:3; Rare:69 | ||||
| chr7:27115276-27115455 | Rare:27 | ||||
| chr7:32728742-32728878 | Common:7; Rare:49 | ||||
| chr7:44107903-44108099 | Common:2; Rare:67; Clinvar (pathogenic):1 | ||||
| chr7:44986602-44986758 | Common:2; Rare:82 | ||||
| chr7:45768893-45769154 | Common:3; Rare:80 |