| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75646753-75647153 | Common:1; Rare:111 | ||||
| chr16:75647520-75648289 | Common:24; Rare:1215; Clinvar:27; Clinvar (pathogenic):6 | ||||
| chr16:75648229-75648873 | Rare:515 | ||||
| chr16:77190622-77191415 | Common:91; Rare:1372 | ||||
| chr16:77191573-77191994 | Common:5; Rare:293 | ||||
| chr16:77212041-77213046 | Common:14; Rare:428 | ||||
| chr16:77212960-77213290 | Common:10; Rare:179 | ||||
| chr16:77722220-77722652 | Common:26; Rare:624 | ||||
| chr16:77722630-77722930 | Common:3; Rare:138 | ||||
| chr16:78099220-78099846 | Common:20; Rare:1201; Clinvar:2; Clinvar (benign):24 | ||||
| chr16:78099939-78100339 | Common:4; Rare:228 | ||||
| chr16:80540394-80541174 | Common:15; Rare:520 | ||||
| chr16:81006228-81007298 | Common:39; Rare:1260 | ||||
| chr16:81007300-81007723 | Common:41; Rare:564 | ||||
| chr16:81035630-81035897 | Common:5; Rare:126 |