chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28809813588098136AG14GENIChomozygous109898700
28809863288098633GA19GENIChomozygous110951678
28809893788098938TG19GENIChomozygous109898702
28810109388101094GA34GENIChomozygous110951680
28810264988102650TC22GENIChomozygous109898704
28810266788102668GT22GENIChomozygous109898706
28810272388102723T23GENIChomozygous127648732
28809944388099444CG11GENICheterozygous131823712
28809944588099446CG10GENICheterozygous131823713
28809944788099448CG10GENICheterozygous131823714
28810277888102779GA26GENIChomozygous109898708
28810441188104412TC26GENIChomozygous109898714
28810557988105580TC18GENIChomozygous109898718
28810582588105825T29GENIChomozygous127648734
28810628188106282GA25GENIChomozygous109898719
28810635988106360TA18GENIChomozygous109898721
28810677588106776AG37GENICpossibly homozygous109898727
28810677988106780TC37GENICpossibly homozygous109898729
28810718988107190TG26GENIChomozygous109898733
28810724888107249AG21GENIChomozygous109898735
28810758288107583AG28GENIChomozygous109898737
28810835788108359AA22GENICpossibly homozygous131803805
28810836888108369AC26GENIChomozygous109898741
28810870288108703GT22GENIChomozygous110951682
28810873088108734GTGC17GENICheterozygous131803806
28810879988108800GA27GENIChomozygous110951684
28810918088109181TC17GENICpossibly homozygous109898742
28810922488109225CA20GENICpossibly homozygous110951686
28811027388110297ATGGCCAGCTTCTTTGTCACCCTC13GENIChomozygous127648735
28811030988110310A15GENIChomozygous127648736
28811049988110500T18GENIChomozygous127648737
28811058588110586TC19GENIChomozygous109898744
28811090388110904GA19GENIChomozygous110951688
28811101788111018T19GENIChomozygous127648738
28811231088112311GT22GENIChomozygous109898748
28810872888108729GC17GENICheterozygous120169175
28809933288099332TC23GENIChomozygous131803804