| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87765911-87766017 | Rare:44 | ||||
| chr16:87951246-87951495 | Common:2; Rare:86 | ||||
| chr16:88570166-88570452 | Common:2; Rare:107 | ||||
| chr16:88663037-88663382 | Common:9; Rare:147 | ||||
| chr16:88706251-88706522 | Common:4; Rare:125 | ||||
| chr16:88856891-88857163 | Common:4; Rare:131; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217632-89217740 | Common:1; Rare:48 | ||||
| chr16:89508274-89508428 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89560540-89560764 | Rare:101 | ||||
| chr16:89657644-89657855 | Common:1; Rare:110 | ||||
| chr16:89686596-89686733 | Common:8; Rare:75 | ||||
| chr16:89816611-89816769 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:89923139-89923357 | Rare:87 | ||||
| chr16:89972478-89972609 | Common:1; Rare:43 | ||||
| chr16:90022594-90022711 | Rare:48 |