chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195631642956316430GC16GENIChomozygous109738376
195631654456316545GT19GENIChomozygous109943862
195631734956317349A15GENIChomozygous129623386
195631822756318228GA12GENICheterozygous135282387
195631822856318229AG12GENICheterozygous135282388
195631879856318799GA17GENIChomozygous110006663
195632046856320469AG16GENIChomozygous109738382
195632903756329038AG15GENIChomozygous109738392
195632457956324580TG16GENIChomozygous109943864
195632484056324841TC27GENIChomozygous109738388
195632596756325968TA16GENIChomozygous109943866
195632746356327464TC21GENIChomozygous109738390
195631871456318762TATATGAGCAGTCAGTCAGTCAGAGGGACACCGTGAAGTAGACCTGAT11GENIChomozygous133332711
195632349256323497CTGGA24GENIChomozygous133332712
195632497956324979GC12GENIChomozygous133332713
195632503556325038AGA14GENIChomozygous133332714
195632053656320537CT17GENIChomozygous110147766
195632592356325924GA17GENIChomozygous109979056
195632956756329568TC15GENIChomozygous119633753
195632957756329578T12GENICheterozygous135281638
195633101556331015CTG11GENIChomozygous129623389
195633101856331021CCC12GENIChomozygous129623390
195633102156331022CA12GENIChomozygous109738396
195633155056331551CT30GENIChomozygous109943870
195633183456331835AG27GENIChomozygous109738400
195633200656332007AG29GENIChomozygous109738404
195633260256332603GT19GENIChomozygous109738408
195633327256333273CT23GENIChomozygous109738410
195633359356333594AG21GENIChomozygous109943872
195633365156333652AT14GENIChomozygous109738412
195633385756333858CT22GENIChomozygous109738414
195633455856334559AG21GENIChomozygous109738416
195633481156334811AAC11GENIChomozygous133332716
195633539956335400CT23GENIChomozygous110147768
195633544156335442GA23GENIChomozygous109738420
195633544356335444AC22GENIChomozygous109738422