| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1308829-1309192 | Common:4; Rare:99 | ||||
| chr16:1309354-1309769 | Rare:154 | ||||
| chr16:1351778-1352020 | Common:2; Rare:118; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1379567-1379819 | Common:2; Rare:106 | ||||
| chr16:1414632-1414904 | Common:4; Rare:91 | ||||
| chr16:1420633-1421078 | Common:3; Rare:173 | ||||
| chr16:1421106-1421329 | Common:6; Rare:50 | ||||
| chr16:1474921-1475209 | Common:5; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:1475373-1475518 | Common:3; Rare:28 | ||||
| chr16:1475541-1475582 | Rare:7 | ||||
| chr16:1493211-1493669 | Common:4; Rare:141 | ||||
| chr16:1493774-1493830 | Rare:7 | ||||
| chr16:1610022-1610103 | Rare:23 | ||||
| chr16:1610291-1610441 | Rare:37 | ||||
| chr16:1610716-1610919 | Common:1; Rare:60; Clinvar:1 |