Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193059275-193059440 | Rare:75 | ||||
chr1:193059447-193059756 | Common:1; Rare:154 | ||||
chr1:193105331-193105485 | Common:2; Rare:66 | ||||
chr1:193186605-193186687 | Rare:16 | ||||
chr1:197146352-197146788 | Common:1; Rare:131; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:197902598-197902652 | Common:1; Rare:17 | ||||
chr1:200669773-200669831 | Rare:18 | ||||
chr1:200669842-200670052 | Common:12; Rare:79 | ||||
chr1:201283277-201283675 | Common:3; Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
chr1:201283677-201283904 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr1:201397281-201397339 | Common:1; Rare:10 | ||||
chr1:201399268-201399758 | Common:1; Rare:173 | ||||
chr1:201469113-201469363 | Common:2; Rare:85 | ||||
chr1:201739703-201739903 | Rare:38 | ||||
chr1:201946180-201946297 | Rare:36 |