| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56917071-56917319 | Rare:37 | ||||
| chr16:56965979-56966090 | Common:2; Rare:17 | ||||
| chr16:56971238-56971533 | Common:3; Rare:75; Clinvar (benign):1 | ||||
| chr16:56980989-56981096 | Rare:12 | ||||
| chr16:56990133-56990259 | Rare:22 | ||||
| chr16:56990492-56990564 | Rare:14 | ||||
| chr16:56990967-56991082 | Common:1; Rare:22 | ||||
| chr16:56991897-56992067 | Common:2; Rare:44 | ||||
| chr16:56999471-56999633 | Rare:27 | ||||
| chr16:57000653-57000917 | Common:5; Rare:46 | ||||
| chr16:57005069-57005140 | Common:1; Rare:12 | ||||
| chr16:57014696-57014873 | Common:2; Rare:35 | ||||
| chr16:57039188-57039335 | Rare:19 | ||||
| chr16:57045870-57045999 | Rare:37 | ||||
| chr16:57135116-57135182 | Rare:4 |