Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38873306-38873540 | Common:3; Rare:81 | ||||
chr1:39026246-39026398 | Common:1; Rare:41 | ||||
chr1:39883480-39883610 | Rare:45 | ||||
chr1:40040463-40040801 | Common:3; Rare:102 | ||||
chr1:40161252-40161402 | Rare:38 | ||||
chr1:40257908-40258303 | Common:4; Rare:108; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40508653-40508816 | Common:4; Rare:44 | ||||
chr1:42456233-42456575 | Common:1; Rare:100 | ||||
chr1:42766562-42766722 | Rare:40; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42766984-42767312 | Common:4; Rare:111; Clinvar (benign):1 | ||||
chr1:42816931-42817146 | Common:1; Rare:60 | ||||
chr1:42817219-42817650 | Rare:127 | ||||
chr1:42846401-42846635 | Common:1; Rare:64 | ||||
chr1:42958827-42959084 | Common:4; Rare:72; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172053-43172341 | Common:3; Rare:111 |