chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57681376876813769CA29GENIChomozygous113871571
57681456076814561AT16GENIChomozygous113871573
57681496176814962GC41GENIChomozygous113871577
57681606476816065CT26GENIChomozygous113871579
57681617476816175GA24GENICpossibly homozygous113871581
57681711576817116CT29GENIChomozygous113871585
57681748876817489TG31GENIChomozygous113871587
57681773076817731TA21GENIChomozygous113871591
57681785576817856AC28GENIChomozygous113871593
57681996676819967TC37GENIChomozygous113871595
57682762276827623TC49GENIChomozygous113871603
57682867576828676TC49GENIChomozygous113871606
57682889376828894CT38GENIChomozygous113871608
57683022276830223CT18GENIChomozygous113871610
57683048376830484CT32GENIChomozygous113871612
57683188876831889AG18GENIChomozygous113871614
57683282176832822CA33GENIChomozygous113871616
57683312576833126GT38GENIChomozygous113871618
57683344776833448CG29GENIChomozygous113871622
57683375376833754CA36GENIChomozygous113871624
57683422176834222TA54GENIChomozygous118843597
57683422276834223AT54GENIChomozygous118843598
57683434676834347TC40GENIChomozygous118843599
57683664676836647TC41GENIChomozygous113871642
57683915276839153TC50GENIChomozygous113871644
57684577176845772CG13GENIChomozygous114126669
57684597376845974GA4GENIChomozygous118843600
57684627976846280GT27GENIChomozygous113871658
57684642476846425AT37GENIChomozygous118843601
57684696476846965AG53GENIChomozygous113871662
57684813476848135TC29GENIChomozygous113871664
57684860076848601AG27GENIChomozygous113871666