| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1964588-1965089 | Common:17; Rare:227 | ||||
| chr16:1971879-1972133 | Common:3; Rare:76 | ||||
| chr16:2009573-2009906 | Common:15; Rare:126 | ||||
| chr16:2047737-2048063 | Rare:165; Clinvar:2; Clinvar (benign):7 | ||||
| chr16:2155319-2155696 | Rare:131 | ||||
| chr16:2155707-2155855 | Common:2; Rare:38 | ||||
| chr16:2223304-2223640 | Rare:133 | ||||
| chr16:2267841-2268193 | Common:1; Rare:157 | ||||
| chr16:2459976-2460145 | Common:1; Rare:48 | ||||
| chr16:2474955-2475154 | Rare:62; Clinvar (benign):1 | ||||
| chr16:2537959-2538086 | Common:2; Rare:50 | ||||
| chr16:2682359-2682780 | Rare:175 | ||||
| chr16:2752263-2752504 | Common:1; Rare:71 | ||||
| chr16:2752564-2752874 | Common:2; Rare:140 | ||||
| chr16:2758501-2758618 | Rare:39 |