| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1971798-1972182 | Common:11; Rare:451 | ||||
| chr16:1983780-1984297 | Common:17; Rare:368; Clinvar (benign):11 | ||||
| chr16:1984437-1984837 | Common:1; Rare:113; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:1990156-1990583 | Common:4; Rare:143 | ||||
| chr16:1992060-1992576 | Common:40; Rare:899 | ||||
| chr16:1992665-1993065 | Rare:213 | ||||
| chr16:2008876-2009276 | Common:3; Rare:95 | ||||
| chr16:2009306-2010060 | Common:89; Rare:905 | ||||
| chr16:2010276-2010378 | Rare:29 | ||||
| chr16:2010285-2010685 | Common:1; Rare:91 | ||||
| chr16:2019759-2020825 | Common:13; Rare:632 | ||||
| chr16:2026604-2027012 | Common:10; Rare:370 | ||||
| chr16:2032483-2032883 | Common:1; Rare:80 | ||||
| chr16:2033293-2033510 | Common:1; Rare:89 | ||||
| chr16:2033431-2033831 | Common:1; Rare:121 |