| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:721076-721172 | Common:2; Rare:22 | ||||
| chr16:740942-741145 | Rare:70 | ||||
| chr16:970851-971194 | Common:7; Rare:156 | ||||
| chr16:980917-981112 | Common:4; Rare:53 | ||||
| chr16:1078618-1078754 | Rare:33 | ||||
| chr16:1309342-1309763 | Rare:153 | ||||
| chr16:1351693-1352148 | Common:2; Rare:197; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:1420705-1420939 | Common:1; Rare:97 | ||||
| chr16:1493263-1493587 | Common:4; Rare:98 | ||||
| chr16:1533486-1533749 | Common:1; Rare:52 | ||||
| chr16:1612042-1612372 | Common:2; Rare:115; Clinvar:1 | ||||
| chr16:1706026-1706648 | Common:5; Rare:176; Clinvar (pathogenic):1 | ||||
| chr16:1764121-1764364 | Rare:85 | ||||
| chr16:1768201-1768586 | Common:1; Rare:153 | ||||
| chr16:1771488-1771868 | Common:3; Rare:154 |