| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1771488-1771905 | Common:7; Rare:323 | ||||
| chr16:1772605-1772919 | Common:8; Rare:258; Clinvar (pathogenic):5 | ||||
| chr16:1772972-1773419 | Common:7; Rare:374; Clinvar (pathogenic):6 | ||||
| chr16:1773371-1773682 | Common:3; Rare:360 | ||||
| chr16:1781717-1782117 | Common:2; Rare:149 | ||||
| chr16:1782341-1783079 | Common:14; Rare:657 | ||||
| chr16:1826460-1827022 | Common:23; Rare:439 | ||||
| chr16:1827110-1827515 | Common:7; Rare:513 | ||||
| chr16:1942225-1942547 | Rare:66 | ||||
| chr16:1943083-1943555 | Common:3; Rare:410 | ||||
| chr16:1959345-1959721 | Common:13; Rare:265 | ||||
| chr16:1964588-1965137 | Common:52; Rare:591 | ||||
| chr16:1971783-1972160 | Common:9; Rare:286 | ||||
| chr16:1972591-1972810 | Common:3; Rare:54 | ||||
| chr16:1983582-1983743 | Common:4; Rare:77 |