chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31249132512491329GTGA54GENIChomozygous127850540
31249163212491633AG72GENIChomozygous111449988
31249179912491800CT64GENICpossibly homozygous119967433
31249269112492692CA49GENIChomozygous111449989
31249329912493300GA56GENIChomozygous119967434
31249492512494926GA59GENIChomozygous119967435
31249548012495480A30GENIChomozygous127850541
31249548212495482AGGA30GENIChomozygous127850542
31249548312495484CA29GENIChomozygous119667067
31249609612496097T6GENIChomozygous127850543
31249611612496117TG6GENIChomozygous111449992
31249760112497602AG64GENIChomozygous111449995
31249791012497911GA67GENIChomozygous111449996
31250060412500605CT30GENIChomozygous111449997
31250061712500618GT27GENIChomozygous111449998
31250156112501562CT41GENIChomozygous111449999
31250202812502029CT32GENIChomozygous119967436
31250270012502701TC48GENIChomozygous119772875
31250383312503834TC55GENIChomozygous111450000
31250497212504973AG58GENIChomozygous111450001
31250569512505696TC58GENIChomozygous111450002
31250632812506329CA52GENIChomozygous111450003
31250656312506564GC59GENIChomozygous111450005
31250660512506606GA62GENICpossibly homozygous119967437
31250668612506687GT62GENICpossibly homozygous111450006
31250684512506846TA67GENIChomozygous111450007
31250686412506865GT70GENIChomozygous111450008
31250755712507558AC38GENIChomozygous111450009
31250760512507605AACC18GENICpossibly homozygous127850545
31250776812507769C47GENIChomozygous127850546
31250810812508109TA63GENIChomozygous111450011
31250828212508283AC60GENICpossibly homozygous119967438
31250837712508378AC54GENIChomozygous111450012
31250897512508976GA51GENIChomozygous119967439
31249701512497029CTCTCCCTGGCCCT62GENIChomozygous135161451
31249764312497769GAAAGGGGCAAGAGGGGCTGGGGATTTAGCTCAGTGGTAGAGTGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAAAAAA71GENIChomozygous131616867