| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15856875-15857183 | Common:3; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:15857275-15857367 | Common:2; Rare:20 | ||||
| chr16:18790291-18790476 | Common:1; Rare:65 | ||||
| chr16:18926114-18926150 | Rare:13 | ||||
| chr16:18926391-18926657 | Common:2; Rare:105 | ||||
| chr16:20806336-20806527 | Rare:68 | ||||
| chr16:20900026-20900840 | Common:6; Rare:186 | ||||
| chr16:21652594-21652624 | Rare:15 | ||||
| chr16:21953028-21953391 | Common:1; Rare:86; Clinvar (benign):1 | ||||
| chr16:22436995-22437320 | Rare:114 | ||||
| chr16:22437364-22437609 | Common:2; Rare:78 | ||||
| chr16:22814768-22815010 | Common:1; Rare:81 | ||||
| chr16:23453154-23453315 | Common:1; Rare:45 | ||||
| chr16:23557318-23557468 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641247-23641525 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):3 |