| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4538392-4538619 | Common:3; Rare:75 | ||||
| chr16:4734190-4734561 | Common:1; Rare:126 | ||||
| chr16:4847236-4847493 | Common:2; Rare:121 | ||||
| chr16:5033615-5033967 | Common:2; Rare:171 | ||||
| chr16:8797607-8797937 | Common:1; Rare:135; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr16:8868979-8869250 | Common:4; Rare:121 | ||||
| chr16:10580578-10580909 | Common:2; Rare:115 | ||||
| chr16:11345251-11345469 | Common:1; Rare:77 | ||||
| chr16:11797134-11797479 | Common:2; Rare:126 | ||||
| chr16:11851477-11851614 | Common:1; Rare:77 | ||||
| chr16:11915370-11915453 | Common:4; Rare:37 | ||||
| chr16:11915895-11915935 | Common:1; Rare:33 | ||||
| chr16:11915944-11916218 | Common:1; Rare:88 | ||||
| chr16:11976604-11976745 | Common:3; Rare:54 | ||||
| chr16:15643019-15643267 | Rare:75 |