| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56191711-56191928 | Common:1; Rare:59 | ||||
| chr16:56192108-56192305 | Common:1; Rare:38; Clinvar (benign):2 | ||||
| chr16:56451280-56451605 | Common:1; Rare:104 | ||||
| chr16:56519975-56520150 | Common:4; Rare:65; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56608472-56608665 | Common:2; Rare:55 | ||||
| chr16:56682351-56682480 | Common:3; Rare:45 | ||||
| chr16:56729958-56730211 | Common:1; Rare:63 | ||||
| chr16:56781581-56781866 | Common:1; Rare:53 | ||||
| chr16:56931939-56932169 | Common:2; Rare:118 | ||||
| chr16:57185804-57186445 | Common:4; Rare:178 | ||||
| chr16:57244938-57245246 | Common:3; Rare:106 | ||||
| chr16:57447344-57447508 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57639283-57639597 | Common:2; Rare:62; Clinvar (pathogenic):1 | ||||
| chr16:57985100-57985169 | Common:1; Rare:32 | ||||
| chr16:58001317-58001463 | Rare:43 |