| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107205813-107205946 | Rare:25 | ||||
| chr7:107211160-107211289 | Rare:44; Clinvar (pathogenic):1 | ||||
| chr7:107229655-107229834 | Common:1; Rare:33 | ||||
| chr7:107298131-107298151 | Rare:7 | ||||
| chr7:107924000-107924386 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):5 | ||||
| chr7:107925926-107926361 | Common:2; Rare:124; Clinvar (benign):1 | ||||
| chr7:107926633-107926686 | Common:1; Rare:12 | ||||
| chr7:107975071-107975307 | Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:107977103-107977344 | Common:6; Rare:36 | ||||
| chr7:108226353-108226525 | Common:1; Rare:36 | ||||
| chr7:108510207-108510216 | |||||
| chr7:108641368-108641371 | |||||
| chr7:109656129-109656153 | Rare:4 | ||||
| chr7:110441506-110441737 | Rare:39 | ||||
| chr7:110534668-110534976 | Common:2; Rare:57 |