| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75464640-75464738 | Rare:34 | ||||
| chr16:75555100-75555500 | Common:4; Rare:85 | ||||
| chr16:75555910-75556005 | Common:1; Rare:37; Clinvar (benign):2 | ||||
| chr16:75566178-75566434 | Common:2; Rare:114 | ||||
| chr16:75622255-75622319 | Rare:12 | ||||
| chr16:75623203-75623440 | Common:4; Rare:89 | ||||
| chr16:75647568-75647936 | Common:4; Rare:170; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648558-75648745 | Rare:81 | ||||
| chr16:77190451-77190564 | Rare:23 | ||||
| chr16:77190630-77191038 | Common:14; Rare:140 | ||||
| chr16:77191105-77191292 | Common:1; Rare:76 | ||||
| chr16:77212972-77213098 | Common:2; Rare:37 | ||||
| chr16:77722300-77722636 | Common:4; Rare:124 | ||||
| chr16:77722680-77722740 | Common:1; Rare:19 | ||||
| chr16:78099251-78099759 | Common:3; Rare:212; Clinvar (benign):4 |