| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:12901700-12901870 | Rare:51 | ||||
| chr16:13919889-13920250 | Common:3; Rare:147; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:14071005-14071375 | Common:4; Rare:127 | ||||
| chr16:14186560-14186736 | Rare:33 | ||||
| chr16:14630144-14630455 | Rare:131 | ||||
| chr16:14632672-14632996 | Common:1; Rare:113 | ||||
| chr16:15094079-15094482 | Common:3; Rare:204 | ||||
| chr16:15434260-15434650 | Common:2; Rare:144 | ||||
| chr16:15434740-15434967 | Common:1; Rare:89 | ||||
| chr16:15642600-15642814 | Common:2; Rare:61 | ||||
| chr16:15642980-15643450 | Common:2; Rare:176; Clinvar:6 | ||||
| chr16:15643506-15643754 | Common:3; Rare:54; Clinvar:6; Clinvar (benign):3 | ||||
| chr16:15649972-15650276 | Common:2; Rare:136 | ||||
| chr16:15672892-15673078 | Common:1; Rare:43 | ||||
| chr16:15888555-15888838 | Common:5; Rare:103 |