| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107195706-107196007 | Common:2; Rare:79 | ||||
| chr7:107563861-107564028 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107580123-107580306 | Common:2; Rare:69 | ||||
| chr7:107743588-107743861 | Common:4; Rare:106 | ||||
| chr7:107744013-107744176 | Rare:51 | ||||
| chr7:108526039-108526442 | Common:5; Rare:122 | ||||
| chr7:108569537-108570013 | Common:3; Rare:171 | ||||
| chr7:112206339-112206795 | Common:2; Rare:161 | ||||
| chr7:112450171-112450491 | Common:6; Rare:95 | ||||
| chr7:112789924-112790118 | Common:1; Rare:59 | ||||
| chr7:114086185-114086506 | Common:2; Rare:123 | ||||
| chr7:116499509-116499862 | Common:3; Rare:121 | ||||
| chr7:116500011-116500304 | Common:3; Rare:75 | ||||
| chr7:116524513-116524786 | Rare:66 | ||||
| chr7:116526225-116526683 | Common:3; Rare:120; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |