| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1772597-1772898 | Common:3; Rare:100; Clinvar (pathogenic):2 | ||||
| chr16:1773110-1773213 | Rare:31 | ||||
| chr16:1782644-1783015 | Common:1; Rare:116 | ||||
| chr16:1793642-1793920 | Common:4; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:1826780-1826982 | Common:3; Rare:64 | ||||
| chr16:1827166-1827521 | Common:3; Rare:183 | ||||
| chr16:1943133-1943513 | Common:1; Rare:122 | ||||
| chr16:1959407-1959662 | Common:5; Rare:111 | ||||
| chr16:1959669-1959752 | Common:1; Rare:36 | ||||
| chr16:1964437-1965074 | Common:19; Rare:269 | ||||
| chr16:1971906-1972110 | Common:1; Rare:59 | ||||
| chr16:2009622-2009896 | Common:15; Rare:108 | ||||
| chr16:2026805-2027112 | Common:3; Rare:93 | ||||
| chr16:2047795-2048058 | Rare:129; Clinvar:2; Clinvar (benign):5 | ||||
| chr16:2155519-2155820 | Common:1; Rare:89 |