| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67278940-67279180 | Common:1; Rare:57 | ||||
| chr16:67279201-67279671 | Common:5; Rare:713 | ||||
| chr16:67326501-67326980 | Common:14; Rare:907 | ||||
| chr16:67393379-67393779 | Common:3; Rare:212 | ||||
| chr16:67396172-67396530 | Common:3; Rare:227 | ||||
| chr16:67430822-67431334 | Common:8; Rare:260; Clinvar (pathogenic):1 | ||||
| chr16:67431290-67432217 | Common:2; Rare:212; Clinvar (pathogenic):1 | ||||
| chr16:67480504-67480692 | Rare:45 | ||||
| chr16:67481041-67481500 | Common:12; Rare:842 | ||||
| chr16:67481568-67482029 | Rare:141 | ||||
| chr16:67528560-67528940 | Rare:348 | ||||
| chr16:67530113-67530513 | Common:1; Rare:103 | ||||
| chr16:67561899-67562280 | Rare:286 | ||||
| chr16:67562200-67562716 | Common:4; Rare:476 | ||||
| chr16:67562640-67563374 | Common:12; Rare:520 |