| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75979081-75979283 | Rare:55; Clinvar:4 | ||||
| chr17:75979374-75979490 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr17:76072487-76072669 | Rare:56 | ||||
| chr17:76103673-76103876 | Common:5; Rare:74 | ||||
| chr17:76353612-76353667 | Rare:20 | ||||
| chr17:76353839-76354086 | Rare:85 | ||||
| chr17:76476962-76477258 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:76493132-76493333 | Common:1; Rare:34 | ||||
| chr17:76501354-76501766 | Common:1; Rare:100; Clinvar (benign):3 | ||||
| chr17:76537906-76537936 | Rare:8 | ||||
| chr17:76725752-76726051 | Rare:83 | ||||
| chr17:76726437-76726903 | Common:5; Rare:177 | ||||
| chr17:76737302-76737687 | Common:4; Rare:140 | ||||
| chr17:76737845-76738075 | Common:3; Rare:65 | ||||
| chr17:77089031-77089320 | Common:6; Rare:72 |