| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71895342-71895574 | Rare:78 | ||||
| chr16:72093579-72093934 | Rare:89 | ||||
| chr16:74296512-74296902 | Common:1; Rare:136 | ||||
| chr16:74607051-74607192 | Rare:83 | ||||
| chr16:74666857-74667177 | Common:4; Rare:99 | ||||
| chr16:74701087-74701343 | Common:2; Rare:50 | ||||
| chr16:75248149-75248278 | Rare:32 | ||||
| chr16:75433336-75433800 | Common:4; Rare:153 | ||||
| chr16:75623229-75623410 | Common:3; Rare:61 | ||||
| chr16:75647605-75647801 | Common:1; Rare:99; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190685-77191026 | Common:10; Rare:111 | ||||
| chr16:77191086-77191231 | Common:2; Rare:59 | ||||
| chr16:81006438-81006558 | Rare:35 | ||||
| chr16:81006825-81007270 | Common:3; Rare:150 | ||||
| chr16:82034984-82035293 | Common:2; Rare:71 |