| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4847258-4847450 | Common:1; Rare:81 | ||||
| chr16:5033933-5033960 | Rare:8 | ||||
| chr16:8674409-8674645 | Common:1; Rare:78; Clinvar:1 | ||||
| chr16:8797607-8797879 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:10744061-10744314 | Common:1; Rare:94 | ||||
| chr16:11345261-11345459 | Common:1; Rare:67 | ||||
| chr16:11586900-11587058 | Common:2; Rare:46 | ||||
| chr16:11742723-11743014 | Common:2; Rare:117 | ||||
| chr16:11797156-11797543 | Common:4; Rare:148 | ||||
| chr16:11851505-11851675 | Rare:85 | ||||
| chr16:11976623-11976758 | Common:2; Rare:47 | ||||
| chr16:14630227-14630410 | Rare:75 | ||||
| chr16:14632719-14632995 | Common:1; Rare:94 | ||||
| chr16:15094187-15094422 | Common:3; Rare:120 | ||||
| chr16:15395965-15396003 | Rare:15 |