Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:752229-752318 | Common:2; Rare:34 | ||||
chr17:1491174-1491333 | Common:1; Rare:44 | ||||
chr17:1516588-1516954 | Common:2; Rare:127 | ||||
chr17:1716149-1716523 | Common:3; Rare:117 | ||||
chr17:1829780-1830100 | Common:8; Rare:135 | ||||
chr17:2029987-2030181 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
chr17:2303334-2303643 | Rare:112 | ||||
chr17:2303724-2303987 | Common:2; Rare:99 | ||||
chr17:2336414-2336553 | Rare:57 | ||||
chr17:2337366-2337516 | Rare:48 | ||||
chr17:2511812-2511935 | Common:2; Rare:35 | ||||
chr17:3636241-3636479 | Common:4; Rare:63; Clinvar (benign):1 | ||||
chr17:3668527-3668821 | Common:3; Rare:118 | ||||
chr17:3723764-3723903 | Common:1; Rare:77 | ||||
chr17:4143010-4143235 | Rare:72 |