| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:47660510-47660726 | Rare:60; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:48244204-48244364 | Common:1; Rare:54 | ||||
| chr16:48244512-48244610 | Rare:25 | ||||
| chr16:48609998-48610358 | Common:3; Rare:120 | ||||
| chr16:50152862-50152973 | Rare:45 | ||||
| chr16:50245935-50246195 | Common:2; Rare:59 | ||||
| chr16:53054828-53055058 | Common:2; Rare:54 | ||||
| chr16:53703806-53704224 | Common:1; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:55509411-55509661 | Common:1; Rare:39 | ||||
| chr16:56450929-56450992 | Rare:14 | ||||
| chr16:56451085-56451763 | Common:5; Rare:221 | ||||
| chr16:56519984-56520195 | Common:5; Rare:78; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56608342-56608770 | Common:4; Rare:123 | ||||
| chr16:56625065-56625345 | Common:2; Rare:50 | ||||
| chr16:56625627-56625863 | Rare:78 |