| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107563894-107564031 | Common:2; Rare:83; Clinvar (benign):4 | ||||
| chr7:107580162-107580286 | Common:2; Rare:50 | ||||
| chr7:107743649-107743814 | Common:3; Rare:71 | ||||
| chr7:107744077-107744171 | Rare:29 | ||||
| chr7:108526099-108526374 | Common:2; Rare:91 | ||||
| chr7:108569563-108569981 | Common:2; Rare:156 | ||||
| chr7:116499521-116499790 | Common:3; Rare:92 | ||||
| chr7:116524495-116524852 | Rare:86 | ||||
| chr7:116526224-116526590 | Common:2; Rare:98; Clinvar:2 | ||||
| chr7:118183965-118184199 | Common:2; Rare:89 | ||||
| chr7:118214557-118214709 | Common:2; Rare:57 | ||||
| chr7:121396193-121396548 | Common:1; Rare:115 | ||||
| chr7:123557773-123557958 | Common:1; Rare:50 | ||||
| chr7:123748928-123749276 | Common:3; Rare:127 | ||||
| chr7:124929795-124929873 | Common:2; Rare:21 |