Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:46923022-46923210 | Common:3; Rare:77; Clinvar:3; Clinvar (benign):9 | ||||
chr17:46979416-46979707 | Common:5; Rare:64 | ||||
chr17:47189235-47189587 | Rare:88 | ||||
chr17:47323868-47324025 | Common:1; Rare:58 | ||||
chr17:47649399-47650097 | Common:2; Rare:240 | ||||
chr17:47650122-47650435 | Rare:110 | ||||
chr17:47650480-47650797 | Common:3; Rare:122 | ||||
chr17:47693750-47694188 | Common:1; Rare:68 | ||||
chr17:47694542-47694654 | Common:2; Rare:26 | ||||
chr17:47695552-47695673 | Common:1; Rare:25 | ||||
chr17:47831461-47831695 | Rare:76 | ||||
chr17:47851161-47851481 | Common:3; Rare:59 | ||||
chr17:47895745-47896066 | Common:3; Rare:91 | ||||
chr17:47941352-47941705 | Rare:95; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48047737-48047845 | Common:1; Rare:29 |