| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159761834-159762067 | Common:4; Rare:118 | ||||
| chr6:159789552-159789977 | Common:4; Rare:146 | ||||
| chr6:159790244-159790559 | Common:8; Rare:111 | ||||
| chr6:162727736-162728064 | Common:3; Rare:92; Clinvar:1 | ||||
| chr6:166342513-166342653 | Common:3; Rare:55 | ||||
| chr6:166999074-166999424 | Common:1; Rare:118 | ||||
| chr6:169702013-169702149 | Common:1; Rare:59 | ||||
| chr6:169751541-169751645 | Rare:38; Clinvar (benign):1 | ||||
| chr6:170554221-170554409 | Common:1; Rare:63 | ||||
| chr7:727249-727313 | Rare:19; Clinvar:1 | ||||
| chr7:975502-975666 | Common:1; Rare:73 | ||||
| chr7:1570018-1570142 | Common:1; Rare:41 | ||||
| chr7:2242177-2242261 | Common:2; Rare:48 | ||||
| chr7:6009021-6009363 | Common:4; Rare:146; Clinvar:9; Clinvar (benign):15 | ||||
| chr7:6399975-6400150 | Rare:45 |