chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108488684084886844TCTT----1GENIChomozygous51524690
108488856784888568A-1GENIChomozygous52391969
108488936284889363TC17GENICheterozygous51524694
108488941284889414AC--20GENIChomozygous51524695
108489092284890923GA23GENIChomozygous51524696
108489127084891271GA25GENIChomozygous51524697
108489243484892435TTAATAAC1GENIChomozygous51524699
108489311884893119GA15GENICpossibly homozygous51524700
108489327184893412AAAGAGCACTACAATGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAAAAAAAAACCTTAAAAAAAA---------------------------------------------------------------------------------------------------------------------------------------------8GENIChomozygous52322467
108489348084893481TA15GENIChomozygous51524701
108489363284893633TC18GENIChomozygous51524702
108489373984893741TT--3GENICheterozygous52162513
108489466384894664TA22GENIChomozygous51524703
108489569784895698CG28GENICpossibly homozygous51524704
108489601384896014C-8GENIChomozygous51524705
108489802484898025TG8GENICpossibly homozygous51524706
108489986384899864T-4GENIChomozygous51524710
108490053284900533GA25GENIChomozygous51524712
108490170984901710CT24GENICpossibly homozygous51524716
108490175084901751T-13GENIChomozygous51524717
108490357784903578AAGTCGTC2GENIChomozygous51524719
108490538384905384GA18GENIChomozygous51524722
108490542184905422AT11GENIChomozygous51524723
108490577484905775AAC7GENICheterozygous51524726
108490609084906091GA14GENICpossibly homozygous51524727
108490795084907951GC15GENIChomozygous51524728
108490807984908080GT18GENIChomozygous51524729
108491140884911409CG16GENIChomozygous51524732
108491275384912754GA17GENIChomozygous51524733
108491353584913536AG5GENIChomozygous51524734
108491423384914234AAG2GENIChomozygous51524735
108491424984914250AAG2GENIChomozygous51524736