chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17569352575693526GT26GENIChomozygous109501865
17569461575694616TC27GENIChomozygous120867054
17569576575695766TC51GENIChomozygous120867055
17569596375695964AG30GENIChomozygous109501869
17569604175696042TC41GENIChomozygous109501870
17569607275696073TC39GENICpossibly homozygous109501871
17569715275697153AT22GENIChomozygous109501874
17569735875697359AG30GENIChomozygous120867056
17569746175697462CT31GENIChomozygous120867057
17569783175697832TC28GENIChomozygous109501876
17569802075698021GA32GENIChomozygous120867058
17569862975698630TC33GENIChomozygous109501878
17569979975699800GA33GENIChomozygous120867059
17570142975701430TG21GENIChomozygous109501879
17570197275701973CA28GENIChomozygous120867060
17570347975703480TA36GENIChomozygous120867061
17570380575703806CT21GENIChomozygous109501881
17570499475704995TC27GENIChomozygous109501883
17570598675705987CA33GENIChomozygous120867062