| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159726948-159727175 | Rare:89 | ||||
| chr6:159761815-159762077 | Common:4; Rare:128 | ||||
| chr6:159789557-159789952 | Common:4; Rare:134 | ||||
| chr6:161273961-161274181 | Rare:42 | ||||
| chr6:166342519-166342653 | Common:3; Rare:51 | ||||
| chr6:166999074-166999404 | Common:1; Rare:112 | ||||
| chr6:169751585-169751645 | Rare:25; Clinvar (benign):1 | ||||
| chr6:170554211-170554412 | Common:1; Rare:65 | ||||
| chr7:727250-727272 | Rare:7; Clinvar:1 | ||||
| chr7:1138233-1138470 | Common:2; Rare:72 | ||||
| chr7:1537145-1537447 | Rare:93 | ||||
| chr7:1570018-1570100 | Common:1; Rare:25 | ||||
| chr7:2242178-2242256 | Common:2; Rare:46 | ||||
| chr7:4775522-4775652 | Common:4; Rare:54; Clinvar:1 | ||||
| chr7:5513742-5513876 | Common:1; Rare:57 |