| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170554211-170554443 | Common:2; Rare:74 | ||||
| chr7:727261-727299 | Rare:9; Clinvar:1 | ||||
| chr7:1055129-1055372 | Common:1; Rare:82 | ||||
| chr7:1088082-1088116 | Rare:5 | ||||
| chr7:1537161-1537467 | Rare:99 | ||||
| chr7:1560747-1560993 | Common:3; Rare:67 | ||||
| chr7:1570018-1570146 | Common:1; Rare:43 | ||||
| chr7:2242171-2242261 | Common:2; Rare:53 | ||||
| chr7:2403278-2403583 | Common:1; Rare:115 | ||||
| chr7:4775369-4775684 | Common:7; Rare:146; Clinvar:1 | ||||
| chr7:5513768-5513882 | Common:1; Rare:46 | ||||
| chr7:6009029-6009280 | Common:3; Rare:96; Clinvar:3; Clinvar (benign):14 | ||||
| chr7:6272556-6272743 | Rare:90 | ||||
| chr7:7566740-7567047 | Common:5; Rare:127 | ||||
| chr7:12211074-12211400 | Common:4; Rare:141 |