Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:63550179-63550513 | Common:2; Rare:74 | ||||
chr17:63700104-63700323 | Common:1; Rare:54 | ||||
chr17:63773516-63773893 | Common:2; Rare:126 | ||||
chr17:64505451-64505565 | Rare:35 | ||||
chr17:64506163-64506395 | Common:3; Rare:111 | ||||
chr17:64506645-64506811 | Common:2; Rare:70 | ||||
chr17:65056581-65056881 | Common:4; Rare:113 | ||||
chr17:67245147-67245273 | Rare:38 | ||||
chr17:67366457-67366688 | Rare:81 | ||||
chr17:67717823-67717959 | Rare:55 | ||||
chr17:68247875-68248115 | Common:5; Rare:102 | ||||
chr17:68291218-68291518 | Common:1; Rare:87 | ||||
chr17:68512302-68512495 | Common:1; Rare:66; Clinvar (benign):1 | ||||
chr17:69327113-69327290 | Common:1; Rare:53 | ||||
chr17:69414627-69414776 | Rare:31 |