Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43270944-43271039 | Rare:22 | ||||
chr1:43358674-43359063 | Common:7; Rare:123 | ||||
chr1:43367961-43368142 | Rare:46 | ||||
chr1:43389763-43389945 | Common:3; Rare:78 | ||||
chr1:44213380-44213491 | Common:1; Rare:22 | ||||
chr1:44674421-44674749 | Common:3; Rare:85 | ||||
chr1:44739674-44739935 | Common:2; Rare:104 | ||||
chr1:44775438-44775607 | Common:1; Rare:66 | ||||
chr1:45012146-45012284 | Rare:54; Clinvar:4 | ||||
chr1:45339959-45340217 | Rare:96; Clinvar:4; Clinvar (benign):4 | ||||
chr1:45340381-45340470 | Common:1; Rare:24; Clinvar:1 | ||||
chr1:45491132-45491447 | Common:2; Rare:81 | ||||
chr1:45500005-45500385 | Common:2; Rare:101; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522089 | Common:1; Rare:101 | ||||
chr1:45550709-45550894 | Common:1; Rare:51 |