chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17998464279984643CCTTTT8GENIChomozygous62134909
17998504379985044CT11GENIChomozygous62685771
17998585179985852GT7GENICpossibly homozygous61445421
17998609879986099AG5GENIChomozygous62685772
17998640579986406AT6GENIChomozygous62685773
17998853179988532GC6GENIChomozygous62685774
17999045379990454AACC3GENIChomozygous62311112
17999066979990670GT9GENIChomozygous61445430
17999191379991914CT8GENIChomozygous62685775
17999384979993850GA5GENIChomozygous61445434
17999388679993887TTG2GENIChomozygous62685776
17999434279994343TG2GENIChomozygous61445435
17999518179995186CCCCC-----6GENIChomozygous62685777
17999524679995248AC--5GENIChomozygous62134918
17999535679995357TC13GENIChomozygous61445437
17999558779995588TC11GENIChomozygous61445438
17999567079995671CCTTTT11GENICpossibly homozygous62134919
17999577479995775GA3GENIChomozygous62685778
17999585879995859TC12GENIChomozygous61445440
17999639579996396TC5GENIChomozygous61445441
17999668579996686AAAC7GENIChomozygous62685779
17999763979997640GA5GENIChomozygous62685780
17999786079997861TC5GENIChomozygous62134921
17999939379999394TC11GENIChomozygous61445444
18000041180000412GA8GENIChomozygous62685781
18000043780000438AG5GENIChomozygous62685782
18000047080000471GGCAGGCAGA8GENIChomozygous61445446
18000178380001784GA4GENIChomozygous62685783
18000452680004527AG16GENIChomozygous61445450
18000479980004800TC4GENIChomozygous62134932
18000567880005679GA14GENIChomozygous62134933
18000575980005761TG--12GENIChomozygous62685784
18000607280006073CT7GENIChomozygous62685785
18000645280006453AG5GENIChomozygous61445454
18000649680006497GC3GENIChomozygous62649501
18000669880006699GT7GENIChomozygous61445455
18000751580007516GC5GENIChomozygous61445459
18000779280007793A-9GENIChomozygous62245205
18000930780009308A-3GENIChomozygous62134940
18001095480010955TC11GENIChomozygous61445461
18001273180012732TC13GENIChomozygous62685786