| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70438718-70438790 | Rare:13 | ||||
| chr16:70438981-70439402 | Common:1; Rare:144 | ||||
| chr16:70439409-70439662 | Rare:64 | ||||
| chr16:70454493-70454924 | Common:6; Rare:151 | ||||
| chr16:70476566-70477068 | Common:2; Rare:90 | ||||
| chr16:70523170-70523328 | Common:2; Rare:38 | ||||
| chr16:70523439-70524099 | Common:3; Rare:220; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70524220-70524546 | Common:2; Rare:84 | ||||
| chr16:70524636-70524698 | Rare:12 | ||||
| chr16:70801050-70801341 | Common:3; Rare:100 | ||||
| chr16:71288829-71289046 | Rare:45 | ||||
| chr16:71289116-71289575 | Common:4; Rare:126 | ||||
| chr16:71289711-71289797 | Rare:18 | ||||
| chr16:71462135-71462373 | Common:3; Rare:89 | ||||
| chr16:71484116-71484434 | Common:2; Rare:86 |