| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71845895-71846029 | Common:2; Rare:43 | ||||
| chr16:71895373-71895584 | Common:1; Rare:73 | ||||
| chr16:72093539-72093993 | Common:1; Rare:116 | ||||
| chr16:74296707-74296987 | Rare:109 | ||||
| chr16:74304126-74304393 | Common:2; Rare:57 | ||||
| chr16:74701119-74701338 | Common:1; Rare:44 | ||||
| chr16:75433288-75433852 | Common:4; Rare:191 | ||||
| chr16:75464374-75464448 | Common:2; Rare:33 | ||||
| chr16:75623229-75623378 | Common:3; Rare:50 | ||||
| chr16:75647614-75647836 | Common:2; Rare:110; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190683-77191010 | Common:11; Rare:108 | ||||
| chr16:77191086-77191230 | Common:2; Rare:59 | ||||
| chr16:79600658-79600947 | Common:2; Rare:88 | ||||
| chr16:80540877-80541040 | Common:3; Rare:64 | ||||
| chr16:81006282-81006558 | Common:3; Rare:65 |