Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40508660-40508810 | Common:4; Rare:43 | ||||
chr1:40691504-40691841 | Common:2; Rare:158 | ||||
chr1:40692051-40692098 | Rare:20 | ||||
chr1:41242106-41242319 | Rare:63 | ||||
chr1:42335095-42335258 | Common:2; Rare:74 | ||||
chr1:42682158-42682465 | Common:2; Rare:81 | ||||
chr1:42766520-42766722 | Rare:52; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:42766996-42767331 | Common:6; Rare:116; Clinvar (benign):1 | ||||
chr1:42817004-42817136 | Common:1; Rare:32 | ||||
chr1:42846412-42846641 | Common:1; Rare:61 | ||||
chr1:42958849-42958979 | Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
chr1:43172214-43172335 | Common:1; Rare:59 | ||||
chr1:43358662-43358986 | Common:7; Rare:102 | ||||
chr1:43367923-43368149 | Rare:55 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 |