chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108890260488902605GA18INTERGENIChomozygous68156758
108890264988902650TG14INTERGENIChomozygous68156762
108890280588902806TG26INTERGENIChomozygous68156765
108890342488903425CG13INTERGENIChomozygous68156769
108890342588903426CG12INTERGENIChomozygous68156772
108890343288903433GA18INTERGENIChomozygous68156775
108890399988904000TG24INTERGENIChomozygous68156777
108890400588904006AG24INTERGENIChomozygous68156780
108890402688904027CT26INTERGENIChomozygous68156783
108890420188904202TA20INTERGENIChomozygous68156786
108890428288904283TA14INTERGENICpossibly homozygous68156789
108890481988904820GC25INTERGENICheterozygous68156794
108890482088904821AT26INTERGENICheterozygous68156797
108890558588905586TC24INTERGENIChomozygous68156805
108890595988905960TC22INTERGENIChomozygous68156808
108890664988906650AT11INTERGENIChomozygous68156811
108890681488906815GA21INTERGENIChomozygous68796675
108890534588905346AC21INTERGENIChomozygous68796666
108890543188905432CT22INTERGENIChomozygous68796669
108890602088906021CG20INTERGENIChomozygous68796672
108890701588907016GA25INTERGENIChomozygous68156814
108890719388907194TC17INTERGENIChomozygous68156820
108890727388907274GT28INTERGENIChomozygous68796678
108890730188907302GA18INTERGENIChomozygous68156823
108892064288920643GT5INTERGENIChomozygous68156980
108892212688922127TC19INTERGENIChomozygous68157020
108893019588930196CT14INTERGENICpossibly homozygous68928880
108891016288910163GA27INTERGENIChomozygous68928876
108892419888924199TA5INTERGENIChomozygous68928878
108892419788924198GA5INTERGENIChomozygous82695755
108893650188936502CT9INTERGENIChomozygous68928882