| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56932350-56933140 | Common:12; Rare:343 | ||||
| chr16:56936708-56937351 | Common:4; Rare:164 | ||||
| chr16:57092290-57092690 | Common:5; Rare:86 | ||||
| chr16:57186001-57186386 | Common:1; Rare:123 | ||||
| chr16:57244908-57245267 | Common:3; Rare:124 | ||||
| chr16:57372276-57372528 | Rare:57 | ||||
| chr16:57447356-57447540 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:57462523-57462713 | Common:1; Rare:76 | ||||
| chr16:57535943-57536349 | Common:2; Rare:149 | ||||
| chr16:57628080-57628400 | Common:2; Rare:73 | ||||
| chr16:57628522-57628726 | Common:4; Rare:52 | ||||
| chr16:57639280-57639572 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
| chr16:57736891-57737016 | Common:1; Rare:21 | ||||
| chr16:57984778-57985236 | Common:10; Rare:220 | ||||
| chr16:57999959-58000359 | Rare:105 |