Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:47895764-47896110 | Common:2; Rare:97 | ||||
chr17:47941348-47941732 | Rare:103; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048039-48048405 | Common:1; Rare:100 | ||||
chr17:48048605-48048813 | Common:4; Rare:29 | ||||
chr17:48054346-48054686 | Rare:63 | ||||
chr17:48107449-48107796 | Common:5; Rare:78 | ||||
chr17:48590193-48590420 | Common:1; Rare:50 | ||||
chr17:48610518-48610705 | Common:1; Rare:63 | ||||
chr17:48908300-48908412 | Common:1; Rare:26 | ||||
chr17:48915826-48916086 | Common:3; Rare:58 | ||||
chr17:48933226-48933436 | Common:1; Rare:58 | ||||
chr17:48944747-48944918 | Common:2; Rare:61 | ||||
chr17:49707877-49707971 | Rare:52 | ||||
chr17:49708148-49708349 | Common:1; Rare:60 | ||||
chr17:49788358-49788745 | Common:2; Rare:118 |