Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:59619572-59619941 | Common:3; Rare:129 | ||||
chr17:59707397-59707766 | Common:3; Rare:97; Clinvar (benign):3 | ||||
chr17:59837678-59838041 | Rare:56 | ||||
chr17:59892891-59893133 | Rare:71 | ||||
chr17:60526169-60526306 | Rare:56 | ||||
chr17:61399547-61399937 | Rare:108 | ||||
chr17:62627331-62627751 | Common:2; Rare:116 | ||||
chr17:62628028-62628164 | Rare:23 | ||||
chr17:63699986-63700029 | Rare:11 | ||||
chr17:63827050-63827412 | Common:5; Rare:94 | ||||
chr17:64506262-64506394 | Common:3; Rare:53 | ||||
chr17:67245170-67245275 | Rare:32 | ||||
chr17:67717746-67717961 | Rare:73 | ||||
chr17:70169374-70169540 | Common:1; Rare:45 | ||||
chr17:73192817-73193087 | Common:15; Rare:111; Clinvar:2; Clinvar (benign):1 |