chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2270833891270833893GG--21GENIChomozygous60184646
2270834199270834200CT18GENIChomozygous60184648
2270834552270834553AT38GENIChomozygous60184650
2270835039270835040TG20GENIChomozygous60184652
2270835223270835224CT21GENIChomozygous60184654
2270835737270835738TC20GENIChomozygous60184656
2270835749270835750AG16GENIChomozygous60184657
2270835779270835780CG23GENIChomozygous59571704
2270836030270836031GGGA9GENICpossibly homozygous60995205
2270836042270836043TTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGC5GENICheterozygous62215775
2270836688270836689AG26GENICpossibly homozygous60184659
2270836992270836993GT22GENIChomozygous60184661
2270837041270837042GA26GENIChomozygous60184663
2270837449270837450CT18GENIChomozygous60184665
2270837581270837582GC21GENIChomozygous60184667
2270837623270837624TG27GENIChomozygous60184669
2270837703270837704AACTCTGTAGG18GENIChomozygous59571707
2270837919270837923ACAC----10GENIChomozygous59571708
2270838447270838451TAAC----25GENIChomozygous60184671
2270838557270838558G-22GENIChomozygous60184673
2270838647270838648GA24GENICpossibly homozygous60184675
2270838692270838693CG24GENIChomozygous60184677
2270839413270839414AATG5GENIChomozygous60995209
2270839552270839553TC15GENIChomozygous60184679
2270839682270839683TTGACA14GENIChomozygous60184680
2270840208270840209GT18GENIChomozygous60184684
2270840623270840624AG15GENIChomozygous59571713
2270841335270841336AT31GENIChomozygous60184686
2270842005270842006TTACAC3GENIChomozygous60995211
2270843061270843062CCT25GENIChomozygous60184688
2270844177270844180TGT---15GENIChomozygous60184690
2270844190270844191GA14GENIChomozygous59571716
2270845511270845512AG16GENIChomozygous60184692
2270846024270846028AAAG----19GENIChomozygous59571717
2270846393270846394CT26GENIChomozygous60184694
2270843609270843610TA19GENIChomozygous59979787
2270838000270838023AAAAAAAAAAAAAAAAAAAAAAA-----------------------11GENICheterozygous60762403