chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28809813588098136AG23GENIChomozygous109898700
28809863288098633GA23GENIChomozygous110951678
28809893788098938TG29GENIChomozygous109898702
28809933288099332TC16GENICpossibly homozygous131803804
28809944388099444CG17GENICheterozygous131823712
28809944588099446CG17GENICpossibly homozygous131823713
28809944788099448CG17GENIChomozygous131823714
28810109388101094GA24GENIChomozygous110951680
28810264988102650TC16GENIChomozygous109898704
28810266788102668GT18GENIChomozygous109898706
28810277888102779GA23GENIChomozygous109898708
28810272388102723T16GENIChomozygous127648732
28810441188104412TC25GENIChomozygous109898714
28810557988105580TC16GENIChomozygous109898718
28810582588105825T29GENIChomozygous127648734
28810628188106282GA22GENIChomozygous109898719
28810635988106360TA25GENIChomozygous109898721
28810677588106776AG27GENIChomozygous109898727
28810677988106780TC28GENIChomozygous109898729
28810718988107190TG22GENIChomozygous109898733
28810724888107249AG21GENIChomozygous109898735
28810758288107583AG30GENIChomozygous109898737
28810835788108359AA21GENIChomozygous131803805
28810836888108369AC22GENIChomozygous109898741
28810870288108703GT23GENICpossibly homozygous110951682
28810872888108729GC21GENICheterozygous120169175
28810873088108734GTGC21GENICheterozygous131803806
28810879988108800GA21GENIChomozygous110951684
28810918088109181TC19GENIChomozygous109898742
28810922488109225CA21GENIChomozygous110951686
28811027388110297ATGGCCAGCTTCTTTGTCACCCTC22GENIChomozygous127648735
28811030988110310A23GENIChomozygous127648736
28811049988110500T35GENICpossibly homozygous127648737
28811058588110586TC30GENIChomozygous109898744
28811090388110904GA16GENIChomozygous110951688
28811101788111018T19GENIChomozygous127648738
28811231088112311GT30GENIChomozygous109898748