Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45500046-45500358 | Common:1; Rare:76; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521706-45522074 | Common:1; Rare:135 | ||||
chr1:45550730-45551086 | Common:3; Rare:87 | ||||
chr1:45583927-45584185 | Common:1; Rare:102 | ||||
chr1:45686466-45686668 | Rare:73 | ||||
chr1:45687036-45687353 | Common:2; Rare:84 | ||||
chr1:45688079-45688243 | Common:1; Rare:50 | ||||
chr1:45750621-45750816 | Rare:71 | ||||
chr1:45803455-45803655 | Common:2; Rare:76 | ||||
chr1:46133037-46133244 | Common:2; Rare:52 | ||||
chr1:46192377-46192546 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
chr1:46194601-46194730 | Common:1; Rare:47; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:46198331-46198525 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46303138-46303774 | Common:3; Rare:189 | ||||
chr1:46340645-46340819 | Common:3; Rare:46 |