chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28809813588098136AG57GENIChomozygous109898700
28809893788098938TG60GENIChomozygous109898702
28810264988102650TC56GENIChomozygous109898704
28810266788102668GT55GENIChomozygous109898706
28810272388102723T63GENIChomozygous127648732
28809876388098763A58GENIChomozygous127648730
28810220988102213AATA58GENIChomozygous127648731
28810277888102779GA61GENIChomozygous109898708
28810310788103108CT50GENIChomozygous109898710
28810355688103557AG57GENIChomozygous109898712
28810369188103691CCA15GENIChomozygous127648733
28810441188104412TC29GENIChomozygous109898714
28810528588105286GA58GENIChomozygous109898716
28810557988105580TC64GENIChomozygous109898718
28810582588105825T61GENICpossibly homozygous127648734
28810628188106282GA55GENIChomozygous109898719
28810635988106360TA52GENIChomozygous109898721
28810636788106368GA53GENIChomozygous109898723
28810640888106409CT53GENIChomozygous109898725
28810677588106776AG72GENIChomozygous109898727
28810677988106780TC68GENIChomozygous109898729
28810696388106964CT72GENIChomozygous109898731
28810718988107190TG71GENIChomozygous109898733
28810724888107249AG63GENIChomozygous109898735
28810758288107583AG61GENIChomozygous109898737
28810816988108170TC80GENIChomozygous109898739
28810836888108369AC36GENIChomozygous109898741
28810918088109181TC38GENIChomozygous109898742
28811027388110297ATGGCCAGCTTCTTTGTCACCCTC77GENIChomozygous127648735
28811030988110310A74GENIChomozygous127648736
28811049988110500T60GENIChomozygous127648737
28811058588110586TC59GENIChomozygous109898744
28811101788111018T57GENIChomozygous127648738
28811109088111091CT71GENIChomozygous109898746
28811231088112311GT53GENIChomozygous109898748