chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1114392258114392259AG15GENIChomozygous120872070
1114394540114394541TA35GENIChomozygous108188445
1114394576114394577GA43GENIChomozygous120906355
1114397453114397454GA38GENIChomozygous108188448
1114398549114398550GT18GENIChomozygous108188451
1114398812114398813GA27GENIChomozygous120872071
1114399222114399223CT29GENIChomozygous108188452
1114400744114400745CT31GENIChomozygous120872072
1114404017114404018CT25GENIChomozygous120872073
1114404336114404337GA28GENIChomozygous120872074
1114405303114405304TC16GENIChomozygous120872075
1114406173114406174TC15GENIChomozygous108188456
1114406842114406843GA35GENIChomozygous120872076
1114408292114408293AG34GENIChomozygous108188458
1114408372114408373TC34GENIChomozygous108188459
1114410204114410205TA27GENIChomozygous108188460
1114410262114410263TC32GENICpossibly homozygous108188461