| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:727228-727303 | Rare:27; Clinvar:1 | ||||
| chr7:727560-727955 | Common:1; Rare:77 | ||||
| chr7:1570012-1570125 | Common:1; Rare:34 | ||||
| chr7:1980303-1980497 | Common:4; Rare:77 | ||||
| chr7:2242171-2242274 | Common:2; Rare:58 | ||||
| chr7:2354061-2354123 | Rare:28 | ||||
| chr7:2403304-2403619 | Common:1; Rare:124 | ||||
| chr7:4775498-4775704 | Common:6; Rare:96; Clinvar:1 | ||||
| chr7:5513732-5513876 | Common:1; Rare:59 | ||||
| chr7:5592651-5592828 | Common:1; Rare:60 | ||||
| chr7:6009029-6009407 | Common:4; Rare:156; Clinvar:5; Clinvar (benign):15 | ||||
| chr7:6059033-6059274 | Common:5; Rare:93 | ||||
| chr7:6104626-6104934 | Common:5; Rare:118 | ||||
| chr7:6272556-6272771 | Common:1; Rare:102 | ||||
| chr7:6447925-6448066 | Common:1; Rare:49 |