| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:649263-649404 | Common:1; Rare:51 | ||||
| chr16:667940-668183 | Common:1; Rare:90 | ||||
| chr16:684329-684476 | Common:3; Rare:80 | ||||
| chr16:740955-741141 | Rare:61 | ||||
| chr16:970856-971196 | Common:7; Rare:153 | ||||
| chr16:1420728-1420957 | Common:1; Rare:93 | ||||
| chr16:1533492-1533694 | Common:1; Rare:39 | ||||
| chr16:1612032-1612362 | Common:2; Rare:111; Clinvar:1 | ||||
| chr16:1706056-1706351 | Common:2; Rare:94 | ||||
| chr16:1773128-1773191 | Rare:11 | ||||
| chr16:1782510-1782643 | Common:3; Rare:50 | ||||
| chr16:1826790-1826949 | Common:3; Rare:48 | ||||
| chr16:1943174-1943508 | Common:1; Rare:103 | ||||
| chr16:1964806-1964992 | Common:6; Rare:86 | ||||
| chr16:2047802-2048050 | Rare:119; Clinvar:2; Clinvar (benign):1 |