| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19067447-19067682 | Common:5; Rare:88; Clinvar:1 | ||||
| chr16:19067773-19067927 | Common:2; Rare:39 | ||||
| chr16:19521722-19521761 | Rare:12 | ||||
| chr16:20676147-20676198 | Rare:9 | ||||
| chr16:20806337-20806542 | Rare:73 | ||||
| chr16:20900226-20900892 | Common:4; Rare:156 | ||||
| chr16:21599370-21599749 | Common:4; Rare:130 | ||||
| chr16:21652602-21652766 | Rare:35 | ||||
| chr16:21953021-21953444 | Common:1; Rare:105; Clinvar (benign):3 | ||||
| chr16:22297773-22297809 | Rare:11 | ||||
| chr16:22297867-22298133 | Common:1; Rare:64 | ||||
| chr16:22436980-22437329 | Rare:122 | ||||
| chr16:22437455-22437671 | Common:2; Rare:55 | ||||
| chr16:23557318-23557557 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641212-23641551 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):3 |