| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89657584-89658130 | Common:4; Rare:274; Clinvar (benign):1 | ||||
| chr16:89686567-89686728 | Common:8; Rare:78 | ||||
| chr16:89686886-89687094 | Common:3; Rare:80 | ||||
| chr16:89687306-89687556 | Rare:83 | ||||
| chr16:89701654-89701813 | Rare:61 | ||||
| chr16:89720857-89721006 | Common:1; Rare:43 | ||||
| chr16:89816613-89816769 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89873482-89873854 | Common:3; Rare:167 | ||||
| chr16:89923171-89923345 | Rare:63 | ||||
| chr16:89948524-89948804 | Common:3; Rare:84 | ||||
| chr16:89972478-89972664 | Common:1; Rare:67 | ||||
| chr16:90019392-90019701 | Common:5; Rare:92 | ||||
| chr16:90022552-90022716 | Common:1; Rare:66 | ||||
| chr17:352506-352626 | Common:2; Rare:28 | ||||
| chr17:352772-352839 | Common:1; Rare:17 |