| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70523527-70523861 | Common:3; Rare:110; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:71808761-71809155 | Common:1; Rare:164 | ||||
| chr16:71845905-71846029 | Common:1; Rare:39 | ||||
| chr16:71895348-71895584 | Common:1; Rare:80 | ||||
| chr16:72008479-72008760 | Common:5; Rare:109; Clinvar (benign):1 | ||||
| chr16:72093518-72093957 | Rare:114 | ||||
| chr16:74296723-74296930 | Rare:88 | ||||
| chr16:74607080-74607326 | Rare:115 | ||||
| chr16:74666902-74667202 | Common:4; Rare:85 | ||||
| chr16:74701140-74701343 | Common:1; Rare:47 | ||||
| chr16:75433305-75433787 | Common:4; Rare:163 | ||||
| chr16:75623229-75623435 | Common:3; Rare:73 | ||||
| chr16:75647628-75647794 | Common:1; Rare:82; Clinvar:4 | ||||
| chr16:77190698-77191231 | Common:12; Rare:181 | ||||
| chr16:79600732-79600932 | Common:1; Rare:58 |