Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44213303-44213527 | Common:2; Rare:49 | ||||
chr1:44674418-44674722 | Common:3; Rare:81 | ||||
chr1:44775462-44775607 | Rare:55 | ||||
chr1:44775802-44775829 | Rare:6 | ||||
chr1:44775833-44776140 | Common:2; Rare:112 | ||||
chr1:44776496-44776773 | Rare:88 | ||||
chr1:44777599-44777903 | Common:2; Rare:75 | ||||
chr1:45010967-45011211 | Common:2; Rare:67 | ||||
chr1:45339957-45340053 | Rare:32 | ||||
chr1:45340114-45340178 | Rare:23 | ||||
chr1:45340381-45340505 | Common:1; Rare:34; Clinvar:1 | ||||
chr1:45500005-45500385 | Common:2; Rare:101; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522074 | Common:1; Rare:98 | ||||
chr1:45583931-45584155 | Rare:90 | ||||
chr1:45687054-45687357 | Common:1; Rare:80 |