| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23557575-23557736 | Rare:52 | ||||
| chr16:23641223-23641557 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23679215-23679339 | Rare:32 | ||||
| chr16:24729607-24729845 | Common:7; Rare:101 | ||||
| chr16:24730025-24730230 | Rare:68 | ||||
| chr16:25015312-25015462 | Common:2; Rare:54 | ||||
| chr16:25111468-25111790 | Common:2; Rare:83 | ||||
| chr16:25257822-25257938 | Common:2; Rare:52 | ||||
| chr16:27268706-27268880 | Common:1; Rare:67 | ||||
| chr16:27313804-27313974 | Common:1; Rare:47 | ||||
| chr16:27549891-27550204 | Common:2; Rare:121 | ||||
| chr16:28822458-28822759 | Common:1; Rare:97 | ||||
| chr16:28823958-28824132 | Common:1; Rare:53 | ||||
| chr16:28843702-28844337 | Common:1; Rare:202; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr16:28844531-28845058 | Common:2; Rare:162; Clinvar:3; Clinvar (benign):7 |