Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:201283161-201283807 | Common:4; Rare:162; Clinvar:4; Clinvar (benign):2 | ||||
chr1:201399292-201399659 | Common:1; Rare:136 | ||||
chr1:201739802-201739903 | Rare:18 | ||||
chr1:201946081-201946390 | Rare:98 | ||||
chr1:201946411-201946793 | Common:3; Rare:58 | ||||
chr1:202010340-202010630 | Common:3; Rare:65 | ||||
chr1:202012537-202012685 | Common:1; Rare:31 | ||||
chr1:203007286-203007401 | Rare:40 | ||||
chr1:203305300-203305609 | Common:3; Rare:85 | ||||
chr1:204828554-204828721 | Rare:76 | ||||
chr1:207032663-207032926 | Common:3; Rare:43 | ||||
chr1:207050980-207051123 | Common:1; Rare:58 | ||||
chr1:207053094-207053317 | Common:1; Rare:62 | ||||
chr1:207321772-207321815 | Rare:10 | ||||
chr1:207322127-207322314 | Rare:61 |