chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197779462197779463AG1GENIChomozygous61682069
1197779599197779600AT4GENIChomozygous61581204
1197779616197779617TC4GENIChomozygous61581205
1197779666197779681TAACTCAGCCCTAGC---------------4GENIChomozygous61797863
1197779761197779762GT10GENICpossibly homozygous61581206
1197780038197780039AG18GENIChomozygous61040768
1197780103197780104TC20GENIChomozygous61040769
1197783194197783195GC25GENIChomozygous61040777
1197783790197783807AAAAAAAAAAAAAAAAA-----------------17GENIChomozygous61797865
1197784440197784441GT22GENIChomozygous61797867
1197786013197786015TT--18GENIChomozygous61797869
1197787720197787721GA31GENIChomozygous61040782
1197787893197787894CT26GENIChomozygous61797871
1197789290197789291CT18GENIChomozygous61797873
1197789774197789775TC26GENIChomozygous61040783
1197791634197791635CCGTGTGT2GENIChomozygous62189183
1197791786197791787T-13GENICheterozygous61581209
1197792095197792096TC15GENIChomozygous61040787
1197793841197793842TTTA21GENIChomozygous61797875
1197795632197795633AG22GENICpossibly homozygous61797877
1197797106197797107TA31GENIChomozygous61040795
1197797239197797240GT33GENIChomozygous61797879
1197797715197797716GA21GENIChomozygous61797881
1197797775197797776CT21GENIChomozygous61040797
1197800327197800328AG17GENIChomozygous61040800
1197800406197800407CT17GENIChomozygous61040801
1197800723197800724CA31GENIChomozygous61317040
1197800724197800725AG31GENIChomozygous61040802
1197801953197801954CT23GENIChomozygous61040806
1197802718197802719TG18GENIChomozygous61040808
1197803867197803868TC32GENIChomozygous61040812
1197805067197805068AAT24GENIChomozygous61797883
1197805870197805871GA21GENIChomozygous61797885
1197805990197805991AG17GENIChomozygous61040826