chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31249132512491329GTGA48GENIChomozygous127850540
31249163212491633AG34GENIChomozygous111449988
31249179912491800CT42GENIChomozygous119967433
31249269112492692CA63GENIChomozygous111449989
31249329912493300GA32GENIChomozygous119967434
31249492512494926GA36GENIChomozygous119967435
31249548012495480A16GENIChomozygous127850541
31249548212495482AGGA15GENIChomozygous127850542
31249548312495484CA13GENIChomozygous119667067
31249760112497602AG23GENIChomozygous111449995
31249791012497911GA42GENIChomozygous111449996
31250060412500605CT30GENIChomozygous111449997
31250061712500618GT28GENIChomozygous111449998
31250156112501562CT27GENIChomozygous111449999
31250202812502029CT23GENIChomozygous119967436
31250383312503834TC51GENIChomozygous111450000
31250497212504973AG45GENIChomozygous111450001
31250569512505696TC39GENIChomozygous111450002
31250632812506329CA43GENIChomozygous111450003
31250656312506564GC52GENIChomozygous111450005
31250660512506606GA51GENIChomozygous119967437
31250668612506687GT51GENIChomozygous111450006
31250684512506846TA50GENICpossibly homozygous111450007
31250686412506865GT46GENIChomozygous111450008
31250755712507558AC29GENIChomozygous111450009
31250760512507605AACC8GENIChomozygous127850545
31250776812507769C42GENIChomozygous127850546
31250810812508109TA50GENICpossibly homozygous111450011
31250828212508283AC60GENIChomozygous119967438
31250837712508378AC52GENIChomozygous111450012
31250897512508976GA40GENIChomozygous119967439
31250270012502701TC28GENIChomozygous119772875