| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:65125954-65126266 | Common:2; Rare:46 | ||||
| chr16:66549677-66550218 | Common:7; Rare:220; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:66551502-66551631 | Rare:25 | ||||
| chr16:66552426-66552674 | Rare:105 | ||||
| chr16:66603768-66603996 | Rare:32 | ||||
| chr16:66604404-66604477 | Rare:20 | ||||
| chr16:66604530-66604763 | Rare:67 | ||||
| chr16:66604858-66605015 | Common:1; Rare:56 | ||||
| chr16:66605088-66605391 | Common:2; Rare:67 | ||||
| chr16:66696543-66696604 | Common:1; Rare:15 | ||||
| chr16:66696621-66697013 | Common:5; Rare:144 | ||||
| chr16:66751485-66751635 | Common:1; Rare:67 | ||||
| chr16:66751738-66752018 | Common:1; Rare:59 | ||||
| chr16:66830192-66830573 | Rare:63 | ||||
| chr16:66830622-66831063 | Common:3; Rare:160 |