| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:578019-578809 | Common:5; Rare:345; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:588527-588883 | Common:1; Rare:91 | ||||
| chr16:589078-589720 | Common:8; Rare:465 | ||||
| chr16:589741-590320 | Common:10; Rare:453 | ||||
| chr16:636091-636528 | Common:12; Rare:313 | ||||
| chr16:636863-637102 | Common:2; Rare:72 | ||||
| chr16:641642-642035 | Common:10; Rare:314 | ||||
| chr16:642040-642549 | Common:2; Rare:315 | ||||
| chr16:642530-642940 | Common:2; Rare:177 | ||||
| chr16:649233-649429 | Common:2; Rare:76 | ||||
| chr16:660800-661135 | Common:45; Rare:266 | ||||
| chr16:667972-668254 | Rare:206 | ||||
| chr16:679701-680212 | Common:24; Rare:349 | ||||
| chr16:680234-680672 | Common:6; Rare:314 | ||||
| chr16:684261-684521 | Common:8; Rare:355 |