| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58629763-58630139 | Common:2; Rare:104 | ||||
| chr16:58734229-58734386 | Common:4; Rare:49 | ||||
| chr16:65122010-65122153 | Common:1; Rare:46 | ||||
| chr16:66366543-66366701 | Common:2; Rare:34 | ||||
| chr16:66549827-66550006 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:66552461-66552679 | Rare:93 | ||||
| chr16:66729039-66729272 | Rare:53 | ||||
| chr16:66751483-66751494 | Rare:2 | ||||
| chr16:66830901-66831067 | Rare:73 | ||||
| chr16:66880376-66880612 | Common:2; Rare:53 | ||||
| chr16:66934345-66934711 | Common:1; Rare:105 | ||||
| chr16:66935389-66935725 | Common:1; Rare:142 | ||||
| chr16:66963691-66963992 | Common:1; Rare:97 | ||||
| chr16:66964351-66964641 | Common:1; Rare:93 | ||||
| chr16:67028978-67029121 | Rare:52 |