chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28809813588098136AG21GENIChomozygous109898700
28809863288098633GA19GENIChomozygous110951678
28809893788098938TG26GENIChomozygous109898702
28809944388099444CG8GENICpossibly homozygous131823712
28809944588099446CG8GENICpossibly homozygous131823713
28809944788099448CG8GENICpossibly homozygous131823714
28810109388101094GA35GENIChomozygous110951680
28810264988102650TC25GENIChomozygous109898704
28810266788102668GT23GENIChomozygous109898706
28809933288099332TC17GENIChomozygous131803804
28810272388102723T24GENIChomozygous127648732
28810277888102779GA27GENIChomozygous109898708
28810441188104412TC23GENIChomozygous109898714
28810557988105580TC24GENIChomozygous109898718
28810582588105825T20GENIChomozygous127648734
28810628188106282GA18GENIChomozygous109898719
28810635988106360TA17GENIChomozygous109898721
28810677588106776AG18GENIChomozygous109898727
28810677988106780TC20GENIChomozygous109898729
28810718988107190TG28GENIChomozygous109898733
28810724888107249AG27GENIChomozygous109898735
28810758288107583AG22GENIChomozygous109898737
28810835788108359AA15GENIChomozygous131803805
28810836888108369AC16GENIChomozygous109898741
28810870288108703GT16GENIChomozygous110951682
28810873088108734GTGC12GENICheterozygous131803806
28811027388110297ATGGCCAGCTTCTTTGTCACCCTC18GENIChomozygous127648735
28811030988110310A19GENIChomozygous127648736
28811049988110500T20GENIChomozygous127648737
28811090388110904GA15GENIChomozygous110951688
28810879988108800GA13GENIChomozygous110951684
28810918088109181TC16GENIChomozygous109898742
28810922488109225CA25GENIChomozygous110951686
28811058588110586TC20GENIChomozygous109898744
28810872888108729GC12GENICheterozygous120169175
28811101788111018T23GENIChomozygous127648738
28811231088112311GT24GENIChomozygous109898748