chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122354503823545039AG23GENIChomozygous813418934
122354722423547225GA32GENIChomozygous813418935
122354791123547912GA12GENIChomozygous813418936
122354791623547917GT10GENIChomozygous813418937
122354792223547923AG9GENIChomozygous813418938
122354794323547944GC9GENICpossibly homozygous813418939
122354794923547950AC11GENICheterozygous813418940
122354796423547965GA8GENICheterozygous813418941
122354824023548241TC29GENIChomozygous813418942
122354918823549189GT29GENIChomozygous813418943
122354923723549238CT50GENIChomozygous813418944
122354965523549656CT55GENIChomozygous813418945
122354971023549711AG29GENIChomozygous813418946
122354987023549871TC29GENIChomozygous813418947
122355010723550108TC36GENIChomozygous813418948
122355016623550167CT29GENIChomozygous813418949
122355037623550377CT63GENIChomozygous813418950
122355109723551098TC19GENIChomozygous813418951
122355130623551307CT19GENICpossibly homozygous813418952
122355152523551526CT25GENIChomozygous813418953
122355233623552337TC35GENIChomozygous813418954
122355254423552545TC27GENIChomozygous813418955
122355261823552619AG44GENIChomozygous813418956
122355269423552695GC75GENICheterozygous813418957
122355344023553441CT32GENIChomozygous813418958
122355391023553911GA30GENIChomozygous813418959
122355433623554337CT36GENIChomozygous813418960
122355466223554663AC46GENICheterozygous813418961
122355616623556167CT25GENIChomozygous813418962
122355668423556685GA33GENICpossibly homozygous813418963
122355674723556748TC32GENIChomozygous813418964
122355679023556791AC27GENIChomozygous813418965
122355690123556902TC16GENIChomozygous813418966
122355805123558052AC42GENIChomozygous813418967
122356027523560276AG27GENIChomozygous813418968
122356327823563279GA29GENIChomozygous813418969
122356338623563387TC39GENIChomozygous813418970