| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87933930-87934331 | Common:3; Rare:167 | ||||
| chr7:88219973-88220243 | Rare:201 | ||||
| chr7:90244930-90245350 | Common:1; Rare:155 | ||||
| chr7:90346550-90346752 | Common:8; Rare:168 | ||||
| chr7:90403312-90403545 | Common:1; Rare:88 | ||||
| chr7:90595822-90596159 | Common:13; Rare:173 | ||||
| chr7:90596226-90596667 | Common:2; Rare:144 | ||||
| chr7:91264140-91264660 | Common:4; Rare:216 | ||||
| chr7:91880661-91880814 | Common:2; Rare:77 | ||||
| chr7:91940706-91941005 | Common:7; Rare:151; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134282-92134598 | Rare:169 | ||||
| chr7:92134717-92134924 | Common:6; Rare:114 | ||||
| chr7:92245799-92246257 | Common:7; Rare:167; Clinvar:7; Clinvar (benign):9 | ||||
| chr7:92447433-92447569 | Common:2; Rare:50 | ||||
| chr7:92528349-92528840 | Common:7; Rare:271; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):3 |