Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:732326-732615 | Common:2; Rare:99 | ||||
chr17:752159-752360 | Common:2; Rare:78 | ||||
chr17:1400108-1400311 | Common:2; Rare:91 | ||||
chr17:1516588-1516954 | Common:2; Rare:127 | ||||
chr17:1716245-1716538 | Common:3; Rare:85 | ||||
chr17:1829786-1830051 | Common:8; Rare:112 | ||||
chr17:2303773-2303987 | Common:2; Rare:77 | ||||
chr17:3636261-3636479 | Common:4; Rare:49; Clinvar (benign):1 | ||||
chr17:3668546-3668837 | Common:2; Rare:115 | ||||
chr17:3723802-3723925 | Rare:68 | ||||
chr17:4143609-4143740 | Common:4; Rare:74 | ||||
chr17:4263943-4264037 | Rare:41 | ||||
chr17:4704117-4704211 | Rare:55 | ||||
chr17:4796130-4796209 | Rare:29 | ||||
chr17:4806999-4807192 | Common:4; Rare:63 |