| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68245101-68245539 | Common:3; Rare:333 | ||||
| chr16:68263950-68264281 | Common:4; Rare:97 | ||||
| chr16:68264345-68264689 | Rare:212 | ||||
| chr16:68265297-68265483 | Rare:28 | ||||
| chr16:68265474-68265672 | Common:2; Rare:34 | ||||
| chr16:68290210-68290670 | Common:6; Rare:202 | ||||
| chr16:68310734-68311167 | Common:11; Rare:473 | ||||
| chr16:68351851-68352351 | Common:4; Rare:169; Clinvar (pathogenic):1 | ||||
| chr16:68448464-68448891 | Common:3; Rare:314 | ||||
| chr16:68529970-68530216 | Common:15; Rare:258 | ||||
| chr16:68539112-68539385 | Common:5; Rare:209 | ||||
| chr16:68644633-68644960 | Common:2; Rare:74; Clinvar:5; Clinvar (benign):2 | ||||
| chr16:68645061-68645433 | Common:1; Rare:120; Clinvar:9 | ||||
| chr16:68645450-68646110 | Common:5; Rare:259; Clinvar:4 | ||||
| chr16:68737098-68737714 | Common:20; Rare:425; Clinvar:29; Clinvar (benign):77 |