| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56425303-56425773 | Common:6; Rare:162 | ||||
| chr16:56450854-56451012 | Common:3; Rare:43 | ||||
| chr16:56451255-56451627 | Common:1; Rare:123 | ||||
| chr16:56451731-56451866 | Rare:36 | ||||
| chr16:56519574-56519840 | Common:1; Rare:103; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:56519922-56520207 | Common:6; Rare:101; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56608371-56608608 | Common:2; Rare:67 | ||||
| chr16:56638480-56638676 | Common:2; Rare:72 | ||||
| chr16:56682272-56682489 | Common:3; Rare:66 | ||||
| chr16:56729838-56730335 | Common:2; Rare:118 | ||||
| chr16:56730478-56730608 | Common:2; Rare:33 | ||||
| chr16:56931663-56931713 | Rare:9 | ||||
| chr16:56931818-56932217 | Common:3; Rare:174 | ||||
| chr16:56932356-56932450 | Rare:30 | ||||
| chr16:56932535-56932702 | Common:2; Rare:39 |