| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151877123-151877535 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:152435673-152435731 | Common:1; Rare:14 | ||||
| chr7:152676094-152676316 | Common:2; Rare:102; Clinvar (benign):7 | ||||
| chr7:155003241-155003480 | Common:6; Rare:96 | ||||
| chr7:155644357-155644897 | Common:6; Rare:174 | ||||
| chr7:156640548-156640729 | Common:2; Rare:89 | ||||
| chr7:157336749-157337106 | Common:3; Rare:171; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158856423-158856703 | Common:7; Rare:99 | ||||
| chr8:232093-232452 | Common:3; Rare:143 | ||||
| chr8:406707-406999 | Common:4; Rare:139 | ||||
| chr8:1755749-1755797 | Rare:15 | ||||
| chr8:2127584-2127811 | Common:7; Rare:42 | ||||
| chr8:6406518-6406683 | Common:3; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563216-6563303 | Common:1; Rare:19 | ||||
| chr8:6708189-6708342 | Common:2; Rare:57 |