| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75433288-75433891 | Common:5; Rare:205 | ||||
| chr16:75464352-75464470 | Common:4; Rare:58 | ||||
| chr16:75555240-75555425 | Common:3; Rare:41 | ||||
| chr16:75556214-75556378 | Common:1; Rare:58; Clinvar (benign):3 | ||||
| chr16:75566192-75566436 | Common:2; Rare:112 | ||||
| chr16:75623208-75623452 | Common:4; Rare:92 | ||||
| chr16:75647584-75647818 | Common:2; Rare:115; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648631-75648671 | Rare:18 | ||||
| chr16:76277110-76277665 | Common:2; Rare:125 | ||||
| chr16:77190686-77191010 | Common:10; Rare:107 | ||||
| chr16:77191133-77191231 | Common:1; Rare:41 | ||||
| chr16:77212165-77212338 | Common:4; Rare:73 | ||||
| chr16:77722314-77722566 | Common:3; Rare:85 | ||||
| chr16:77788277-77788628 | Common:3; Rare:126 | ||||
| chr16:78099290-78099760 | Common:3; Rare:195; Clinvar (benign):4 |