| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69339524-69339871 | Common:1; Rare:153; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:69385676-69386156 | Rare:153 | ||||
| chr16:69424295-69424836 | Common:3; Rare:150 | ||||
| chr16:69565694-69566322 | Common:6; Rare:215 | ||||
| chr16:69726428-69726856 | Common:4; Rare:116 | ||||
| chr16:69754841-69755155 | Common:1; Rare:114 | ||||
| chr16:69762219-69762390 | Common:2; Rare:52 | ||||
| chr16:70114097-70114430 | Common:3; Rare:111 | ||||
| chr16:70289395-70289740 | Rare:125; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:70298965-70299259 | Common:1; Rare:53 | ||||
| chr16:70346751-70346986 | Common:2; Rare:118 | ||||
| chr16:70454324-70454638 | Common:2; Rare:85 | ||||
| chr16:70523223-70523304 | Rare:16 | ||||
| chr16:70523450-70523907 | Common:3; Rare:164; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70685977-70686014 | Rare:16 |