| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75566268-75566431 | Common:1; Rare:87 | ||||
| chr16:75566760-75566907 | Common:2; Rare:62 | ||||
| chr16:75623216-75623372 | Common:3; Rare:60 | ||||
| chr16:75647601-75647818 | Common:2; Rare:107; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648207-75648510 | Rare:102 | ||||
| chr16:77190707-77191057 | Common:10; Rare:112 | ||||
| chr16:77191086-77191321 | Common:2; Rare:91 | ||||
| chr16:79599805-79599854 | Rare:8 | ||||
| chr16:79599982-79600205 | Common:4; Rare:67 | ||||
| chr16:79600666-79600898 | Common:2; Rare:71 | ||||
| chr16:80540925-80541051 | Common:3; Rare:53 | ||||
| chr16:81006430-81006565 | Rare:40 | ||||
| chr16:81006774-81007272 | Common:5; Rare:170 | ||||
| chr16:81077194-81077319 | Common:1; Rare:56 | ||||
| chr16:81238488-81238697 | Common:1; Rare:48 |