Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:56833922-56834231 | Common:3; Rare:108 | ||||
chr17:56960707-56960773 | Rare:30 | ||||
chr17:56960870-56960940 | Rare:19 | ||||
chr17:56960942-56961169 | Common:3; Rare:77 | ||||
chr17:57084956-57085387 | Common:2; Rare:135 | ||||
chr17:57256921-57257059 | Rare:44 | ||||
chr17:57850002-57850292 | Common:1; Rare:95 | ||||
chr17:57988107-57988519 | Common:6; Rare:119 | ||||
chr17:58006351-58006705 | Common:2; Rare:98 | ||||
chr17:58007102-58007390 | Common:1; Rare:127 | ||||
chr17:58007614-58007740 | Rare:32 | ||||
chr17:58219155-58219374 | Common:1; Rare:88; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr17:58328044-58328296 | Rare:49 | ||||
chr17:58328507-58329054 | Common:2; Rare:114 | ||||
chr17:58352131-58352495 | Common:6; Rare:138 |