chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28809813588098136AG61GENIChomozygous109898700
28809863288098633GA63GENIChomozygous110951678
28809893788098938TG54GENIChomozygous109898702
28809944388099444CG14GENICheterozygous131823712
28809944588099446CG15GENIChomozygous131823713
28809944788099448CG15GENIChomozygous131823714
28810109388101094GA52GENIChomozygous110951680
28809933288099332TC44GENICpossibly homozygous131803804
28810264988102650TC46GENIChomozygous109898704
28810266788102668GT47GENIChomozygous109898706
28810272388102723T43GENIChomozygous127648732
28810277888102779GA51GENIChomozygous109898708
28810441188104412TC42GENIChomozygous109898714
28810557988105580TC51GENIChomozygous109898718
28810582588105825T54GENIChomozygous127648734
28810628188106282GA56GENIChomozygous109898719
28810635988106360TA52GENIChomozygous109898721
28810677588106776AG59GENIChomozygous109898727
28810677988106780TC57GENIChomozygous109898729
28810718988107190TG58GENIChomozygous109898733
28810724888107249AG44GENIChomozygous109898735
28810758288107583AG61GENIChomozygous109898737
28810835788108359AA60GENIChomozygous131803805
28810836888108369AC67GENIChomozygous109898741
28810870288108703GT57GENIChomozygous110951682
28811027388110297ATGGCCAGCTTCTTTGTCACCCTC47GENIChomozygous127648735
28811030988110310A42GENIChomozygous127648736
28811049988110500T44GENIChomozygous127648737
28811101788111018T50GENICpossibly homozygous127648738
28811231088112311GT48GENIChomozygous109898748
28810879988108800GA57GENIChomozygous110951684
28810918088109181TC43GENIChomozygous109898742
28810922488109225CA49GENIChomozygous110951686
28811058588110586TC54GENIChomozygous109898744
28811090388110904GA57GENIChomozygous110951688