chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206650348206650349AG32GENIChomozygous61067523
1206650370206650371AAAC32GENIChomozygous61067524
1206650803206650804GA27GENIChomozygous61067525
1206651096206651097GA41GENIChomozygous61067526
1206652948206652949GGA12GENICpossibly homozygous62096210
1206653027206653035TGTGTGTC--------7GENICheterozygous62314594
1206653029206653035TGTGTC------5GENICheterozygous62192986
1206654412206654413AC34GENIChomozygous61067527
1206658200206658212TATCTATGTATC------------18GENIChomozygous62192988
1206658280206658281CCATCT19GENIChomozygous61067528
1206661128206661129GA34GENIChomozygous61067529
1206661774206661775A-30GENIChomozygous61067530
1206662661206662662TTCA11GENIChomozygous61067531
1206664470206664480CTCCCTCTCT----------15GENICpossibly homozygous62192990
1206664574206664576AC--25GENIChomozygous61067532
1206664613206664614CCACATAT24GENIChomozygous61067533
1206664641206664647TATATA------22GENICheterozygous62192992
1206664710206664711AG19GENIChomozygous61067537
1206665220206665223TAC---10GENIChomozygous61067538
1206666699206666700GA22GENIChomozygous61067539
1206668089206668090GA23GENIChomozygous61067540
1206668764206668776GTGTGTGTATGT------------14GENICheterozygous62192994