chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103623547536235476CT57GENIChomozygous51412664
103623560636235608AA--2GENIChomozygous51412666
103623598036235981AATGTGTATAGCCT26GENIChomozygous51412668
103623811536238116CT57GENIChomozygous51412670
103624257436242575TC78GENIChomozygous51412672
103624264336242644AG73GENIChomozygous51412673
103624265736242658GC70GENIChomozygous51412674
103624269636242697GA73GENIChomozygous51412676
103624299136242992TC47GENIChomozygous51412678
103624305336243054TC58GENIChomozygous51412679
103624306836243069TG68GENIChomozygous51412681
103624318736243188CT57GENICpossibly homozygous51412682
103624356836243571GAT---23GENIChomozygous51412684
103624405736244058CA51GENIChomozygous51412686
103624427336244274AG48GENIChomozygous51412687
103624453136244532TTCA12GENIChomozygous51412689
103624582036245821TTA55GENIChomozygous51412691
103624588236245883CT63GENIChomozygous51412693
103624693036246931A-18GENIChomozygous51412695
103624693836246939G-20GENICheterozygous51412697
103624694536246947AA--11GENICheterozygous51412701
103624702736247028CT48GENIChomozygous51412703
103624746036247461TC61GENIChomozygous51412705
103624849336248495CT--23GENIChomozygous51412707
103624849836248499AAAGAGT21GENIChomozygous51412708
103624863836248646TTTGTTTG--------6GENIChomozygous51412710
103624879136248792GGCC27GENIChomozygous51412712
103624925336249254TC36GENIChomozygous51412714
103624941936249420CT48GENIChomozygous51412716
103624945436249455AAT40GENICpossibly homozygous51412718
103625008636250087T-47GENIChomozygous51412720
103625090536250906GA46GENICpossibly homozygous51412722
103624945436249455AATT40GENICheterozygous51634373
103624445936244460AAGCT5GENICheterozygous51634372