| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:14630080-14630590 | Rare:1023 | ||||
| chr16:14632119-14632519 | Common:2; Rare:146 | ||||
| chr16:14632575-14633072 | Common:6; Rare:640 | ||||
| chr16:14633095-14633520 | Rare:351 | ||||
| chr16:14973866-14974266 | Rare:44 | ||||
| chr16:14974601-14975595 | Common:12; Rare:558 | ||||
| chr16:15055900-15056390 | Common:6; Rare:412 | ||||
| chr16:15094065-15094471 | Common:15; Rare:930 | ||||
| chr16:15502270-15502710 | Common:4; Rare:238 | ||||
| chr16:15576270-15576670 | Common:4; Rare:76 | ||||
| chr16:15576738-15577219 | Common:22; Rare:435 | ||||
| chr16:15641720-15642120 | Common:1; Rare:98 | ||||
| chr16:15642471-15643422 | Common:18; Rare:1355; Clinvar:17 | ||||
| chr16:15643481-15644109 | Common:5; Rare:201; Clinvar:16; Clinvar (benign):3 | ||||
| chr16:15649965-15650394 | Common:10; Rare:800 |