| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:72093467-72093957 | Rare:126 | ||||
| chr16:74296460-74296882 | Common:1; Rare:131 | ||||
| chr16:74421766-74422145 | Common:3; Rare:42 | ||||
| chr16:74607093-74607206 | Rare:58 | ||||
| chr16:74666862-74667091 | Common:1; Rare:75 | ||||
| chr16:75433408-75433884 | Common:4; Rare:148 | ||||
| chr16:75556180-75556354 | Common:3; Rare:64; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr16:75566267-75566431 | Common:1; Rare:87 | ||||
| chr16:75623216-75623435 | Common:3; Rare:84 | ||||
| chr16:75647628-75647794 | Common:1; Rare:82; Clinvar:4 | ||||
| chr16:77190683-77191010 | Common:11; Rare:108 | ||||
| chr16:77191086-77191224 | Common:2; Rare:58 | ||||
| chr16:78099308-78099632 | Common:2; Rare:113 | ||||
| chr16:79600729-79600892 | Common:1; Rare:48 | ||||
| chr16:80540828-80541058 | Common:5; Rare:96 |