chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103623481036234818AGAGAGAG--------8GENICheterozygous52367784
103623481236234818AGAGAG------8GENICheterozygous52435654
103623547536235476CT16GENIChomozygous51412664
103623560636235608AA--3GENIChomozygous51412666
103623598036235981AATGTGTATAGCCT34GENIChomozygous51412668
103623811536238116CT26GENIChomozygous51412670
103624257436242575TC30GENIChomozygous51412672
103624264336242644AG25GENIChomozygous51412673
103624265736242658GC23GENIChomozygous51412674
103624269636242697GA20GENIChomozygous51412676
103624299136242992TC10GENIChomozygous51412678
103624305336243054TC24GENIChomozygous51412679
103624306836243069TG25GENIChomozygous51412681
103624318736243188CT27GENIChomozygous51412682
103624356836243571GAT---17GENIChomozygous51412684
103624405736244058CA23GENIChomozygous51412686
103624427336244274AG11GENIChomozygous51412687
103624453136244532TTCA5GENIChomozygous51412689
103624582036245821TTA22GENIChomozygous51412691
103624588236245883CT26GENIChomozygous51412693
103624693036246931A-14GENIChomozygous51412695
103624694436246947AAA---8GENICheterozygous52367795
103624694536246947AA--8GENICheterozygous51412701
103624702736247028CT20GENIChomozygous51412703
103624746036247461TC18GENIChomozygous51412705
103624849336248495CT--22GENIChomozygous51412707
103624849836248499AAAGAGT21GENIChomozygous51412708
103624863836248646TTTGTTTG--------12GENIChomozygous51412710
103624879136248792GGCC13GENIChomozygous51412712
103624925336249254TC36GENIChomozygous51412714
103624941936249420CT41GENIChomozygous51412716
103624945436249455AAT26GENICpossibly homozygous51412718
103625008636250087T-6GENIChomozygous51412720
103624384736243848GGAGATAGAT4GENIChomozygous52493596
103624442636244430CACA----1GENIChomozygous52493598
103624962336249624TTTTTTGTTTTG13GENIChomozygous52493600