| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8868986-8869227 | Common:4; Rare:110 | ||||
| chr16:10580574-10580710 | Rare:46 | ||||
| chr16:10580825-10580878 | Rare:18 | ||||
| chr16:10743801-10743880 | Rare:33 | ||||
| chr16:11797187-11797503 | Common:2; Rare:121 | ||||
| chr16:11851517-11851635 | Rare:57 | ||||
| chr16:11915500-11915605 | Common:1; Rare:36 | ||||
| chr16:11915883-11916215 | Common:2; Rare:137 | ||||
| chr16:11976421-11976766 | Common:5; Rare:122 | ||||
| chr16:14186608-14186823 | Rare:35 | ||||
| chr16:14974873-14975202 | Common:2; Rare:91 | ||||
| chr16:15094229-15094389 | Common:1; Rare:84 | ||||
| chr16:15395912-15396014 | Rare:36 | ||||
| chr16:15643034-15643309 | Common:1; Rare:101; Clinvar:1 | ||||
| chr16:15856946-15857117 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):2 |