chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85874561058745611CT18GENIChomozygous53272075
85874734558747346CT10GENIChomozygous52982552
85874868558748686CCTA14GENIChomozygous53272076
85874902158749022CT11GENIChomozygous53272077
85874906958749070TC15GENIChomozygous52661648
85875022558750226CT12GENIChomozygous53272078
85875134058751341GA16GENIChomozygous52982558
85875142258751423CCA23GENIChomozygous52661650
85875252158752522TG9GENIChomozygous52661652
85875409658754097TC11GENIChomozygous52982562
85875544658755447A-10GENICheterozygous52982564
85875890558758906AAT24GENIChomozygous52982566
85875899958759000A-15GENIChomozygous52982567
85875956958759570GA26GENIChomozygous53272079
85876066058760661GA28GENICpossibly homozygous52982570
85876108258761083AG19GENIChomozygous52661654
85876116258761163CT13GENIChomozygous52982571
85876122258761223GT11GENIChomozygous53272080
85876212558762126CT24GENIChomozygous53272081
85876243158762432GA15GENIChomozygous52982573
85876352058763521TC18GENIChomozygous52661660
85876359658763597CCT19GENICpossibly homozygous52661664
85876392958763930GA31GENICheterozygous53272082
85876392958763930GGAAGA25GENIChomozygous53272083
85876431658764317AG26GENIChomozygous52661668
85876433758764338T-20GENIChomozygous52661670
85876623158766232TTTGTGTGTG10GENICheterozygous52661672
85876625358766254AG18GENICpossibly homozygous52661674
85876671758766718TC9GENIChomozygous52661676
85876784058767841TG12GENIChomozygous53272084
85876849058768491TC15GENICpossibly homozygous52661678
85876915558769156GA21GENICheterozygous52982580
85876963858769639CT21GENIChomozygous52982581
85877009858770099C-9GENIChomozygous52982582
85877059758770598CA21GENIChomozygous52982584