| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71808774-71808869 | Common:1; Rare:53 | ||||
| chr16:71809053-71809120 | Rare:33 | ||||
| chr16:71845916-71846023 | Common:1; Rare:34 | ||||
| chr16:71895241-71895574 | Common:2; Rare:132 | ||||
| chr16:72093548-72093934 | Rare:99 | ||||
| chr16:74296460-74296902 | Common:1; Rare:145 | ||||
| chr16:74607080-74607185 | Rare:58 | ||||
| chr16:74666857-74667168 | Common:4; Rare:99 | ||||
| chr16:74701112-74701343 | Common:1; Rare:50 | ||||
| chr16:75433353-75433795 | Common:4; Rare:145 | ||||
| chr16:75555266-75555420 | Common:1; Rare:35 | ||||
| chr16:75556214-75556384 | Common:1; Rare:64; Clinvar (benign):3 | ||||
| chr16:75647601-75647792 | Common:1; Rare:95; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190702-77191010 | Common:10; Rare:101 | ||||
| chr16:77191110-77191231 | Common:1; Rare:51 |