Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:48527507-48527734 | Rare:34 | ||||
chr17:48546591-48546745 | Rare:33 | ||||
chr17:48555743-48555861 | Rare:28 | ||||
chr17:48578380-48578425 | Common:1; Rare:12 | ||||
chr17:48995994-48996319 | Rare:106 | ||||
chr17:48996485-48996610 | Common:1; Rare:27 | ||||
chr17:49192948-49193123 | Common:1; Rare:41 | ||||
chr17:49691114-49691394 | Common:3; Rare:61 | ||||
chr17:50189395-50189683 | Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
chr17:50583754-50583928 | Rare:32 | ||||
chr17:50944615-50944788 | Rare:40 | ||||
chr17:56597441-56597757 | Common:1; Rare:73 | ||||
chr17:57851784-57851983 | Common:1; Rare:32 | ||||
chr17:58324380-58324585 | Common:1; Rare:55 | ||||
chr17:58631821-58632129 | Common:3; Rare:138 |