| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71895253-71895584 | Common:3; Rare:126 | ||||
| chr16:72093591-72093978 | Common:1; Rare:92 | ||||
| chr16:74296718-74296919 | Rare:84 | ||||
| chr16:74304109-74304381 | Common:2; Rare:57 | ||||
| chr16:74607082-74607194 | Rare:60 | ||||
| chr16:75433303-75433798 | Common:4; Rare:168 | ||||
| chr16:75556214-75556455 | Common:1; Rare:85; Clinvar (benign):3 | ||||
| chr16:75647614-75647848 | Common:3; Rare:118; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190707-77191042 | Common:10; Rare:108 | ||||
| chr16:79600695-79600947 | Common:1; Rare:73 | ||||
| chr16:81006337-81006553 | Common:2; Rare:52 | ||||
| chr16:81006798-81007228 | Common:5; Rare:141 | ||||
| chr16:81610187-81610502 | Common:2; Rare:87 | ||||
| chr16:84116770-84117058 | Common:4; Rare:112 | ||||
| chr16:84145136-84145310 | Common:1; Rare:83; Clinvar:3 |