Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26410680-26410851 | Rare:45 | ||||
chr1:26432091-26432433 | Common:5; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472071-26472627 | Common:5; Rare:180 | ||||
chr1:26473047-26473270 | Rare:116 | ||||
chr1:26529607-26529850 | Common:2; Rare:88 | ||||
chr1:26695713-26696059 | Common:1; Rare:110 | ||||
chr1:26727519-26727750 | Common:2; Rare:42 | ||||
chr1:26775324-26775705 | Common:1; Rare:77; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:26787851-26788243 | Common:3; Rare:115; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890220-26890328 | Common:1; Rare:45 | ||||
chr1:26900411-26900586 | Rare:61 | ||||
chr1:26921548-26921904 | Common:3; Rare:112 | ||||
chr1:26960419-26960493 | Common:1; Rare:12 | ||||
chr1:27234473-27234912 | Common:4; Rare:130 | ||||
chr1:27322020-27322343 | Common:1; Rare:115 |