Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193105373-193105529 | Common:3; Rare:67 | ||||
chr1:193121743-193122216 | Common:2; Rare:171; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:200410005-200410372 | Rare:96 | ||||
chr1:200620732-200620839 | Rare:24 | ||||
chr1:200669809-200670131 | Common:12; Rare:101 | ||||
chr1:200739406-200739736 | Common:1; Rare:91 | ||||
chr1:201283270-201283910 | Common:4; Rare:179; Clinvar:5; Clinvar (benign):2 | ||||
chr1:201284093-201284421 | Common:2; Rare:46 | ||||
chr1:201315624-201316008 | Common:1; Rare:52 | ||||
chr1:201396990-201397297 | Common:3; Rare:61 | ||||
chr1:201399267-201399726 | Common:1; Rare:163 | ||||
chr1:201496264-201496359 | Rare:28 | ||||
chr1:201946363-201946404 | Rare:13 | ||||
chr1:201946473-201946793 | Common:2; Rare:52 | ||||
chr1:201955378-201955539 | Rare:49 |