| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31459091-31459188 | Rare:31 | ||||
| chr16:31459319-31459517 | Common:1; Rare:83 | ||||
| chr16:31471950-31472186 | Rare:54 | ||||
| chr16:31508357-31508484 | Common:2; Rare:54 | ||||
| chr16:46689130-46689354 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689378-46689708 | Common:3; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46831087-46831288 | Common:2; Rare:76 | ||||
| chr16:46884056-46884367 | Common:2; Rare:79 | ||||
| chr16:46973581-46973757 | Rare:78 | ||||
| chr16:47461012-47461374 | Common:2; Rare:144; Clinvar (benign):2 | ||||
| chr16:48244165-48244222 | Common:1; Rare:23 | ||||
| chr16:48244224-48244621 | Common:2; Rare:112 | ||||
| chr16:48347846-48348205 | Common:1; Rare:65 | ||||
| chr16:50693482-50693619 | Rare:56 | ||||
| chr16:50741737-50742162 | Common:7; Rare:129; Clinvar:1 |