Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:35557369-35557442 | Rare:16 | ||||
chr1:35557594-35557850 | Common:2; Rare:100 | ||||
chr1:37859569-37859764 | Common:3; Rare:64 | ||||
chr1:37989961-37990182 | Rare:78 | ||||
chr1:39026246-39026397 | Common:1; Rare:41 | ||||
chr1:39883456-39883575 | Common:1; Rare:49; Clinvar (pathogenic):1 | ||||
chr1:40161231-40161402 | Common:1; Rare:47 | ||||
chr1:40257895-40258255 | Common:4; Rare:95; Clinvar:7 | ||||
chr1:40508679-40508773 | Common:3; Rare:26 | ||||
chr1:40691586-40691810 | Common:1; Rare:111 | ||||
chr1:42335187-42335346 | Common:3; Rare:83 | ||||
chr1:42766996-42767309 | Common:4; Rare:105; Clinvar (benign):1 | ||||
chr1:42846445-42846634 | Common:1; Rare:52 | ||||
chr1:42958830-42959078 | Common:4; Rare:70; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43358662-43358986 | Common:7; Rare:102 |