chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197779462197779463AG20GENIChomozygous61682069
1197779599197779600AT23GENIChomozygous61581204
1197779616197779617TC20GENIChomozygous61581205
1197779666197779681TAACTCAGCCCTAGC---------------23GENIChomozygous61797863
1197779761197779762GT25GENICpossibly homozygous61581206
1197780038197780039AG22GENIChomozygous61040768
1197780103197780104TC24GENIChomozygous61040769
1197783194197783195GC28GENIChomozygous61040777
1197783790197783807AAAAAAAAAAAAAAAAA-----------------27GENICpossibly homozygous61797865
1197784440197784441GT25GENICpossibly homozygous61797867
1197786013197786015TT--19GENIChomozygous61797869
1197787720197787721GA25GENIChomozygous61040782
1197787893197787894CT28GENIChomozygous61797871
1197789290197789291CT31GENIChomozygous61797873
1197789774197789775TC27GENIChomozygous61040783
1197782765197782766CCT6GENICheterozygous62189179
1197791634197791635CCGTGT9GENICheterozygous62189181
1197791634197791635CCGTGTGT9GENICheterozygous62189183
1197792095197792096TC25GENIChomozygous61040787
1197793841197793842TTTA29GENIChomozygous61797875
1197795632197795633AG24GENIChomozygous61797877
1197797106197797107TA33GENIChomozygous61040795
1197797239197797240GT27GENIChomozygous61797879
1197797715197797716GA17GENIChomozygous61797881
1197797775197797776CT19GENIChomozygous61040797
1197800327197800328AG30GENIChomozygous61040800
1197800406197800407CT31GENIChomozygous61040801
1197800723197800724CA28GENIChomozygous61317040
1197800724197800725AG27GENIChomozygous61040802
1197801953197801954CT44GENIChomozygous61040806
1197802718197802719TG22GENIChomozygous61040808
1197803867197803868TC23GENIChomozygous61040812
1197805067197805068AAT23GENIChomozygous61797883
1197805870197805871GA24GENIChomozygous61797885
1197805990197805991AG15GENIChomozygous61040826