chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205960328205960329G-3GENIChomozygous61065912
1205960336205960339TTG---1GENIChomozygous61065913
1205961528205961529CT5GENIChomozygous61065917
1205962491205962492AG17GENICpossibly homozygous61065918
1205963051205963052TC14GENIChomozygous61065919
1205963203205963204GC13GENIChomozygous61065920
1205963384205963385GGA6GENIChomozygous61065921
1205963593205963594A-1GENIChomozygous61065923
1205963919205963920TC11GENICpossibly homozygous61065924
1205964285205964286GA11GENICheterozygous61065926
1205964402205964403AAT5GENICheterozygous61065927
1205964510205964511AG21GENICpossibly homozygous61065928
1205965266205965267A-1GENIChomozygous61065929
1205965702205965703TTA2GENICheterozygous61065930
1205965702205965703TTAA2GENICheterozygous62095851
1205966908205966909GA13GENICheterozygous61065931
1205967347205967348CCT1GENIChomozygous62192719
1205967626205967630AAAT----1GENIChomozygous61065933
1205968469205968470GA27GENICpossibly homozygous61065938
1205980171205980172GA1GENIChomozygous61065947
1205980247205980248GT18GENIChomozygous61065948
1205982040205982042TA--3GENIChomozygous61065949
1205984175205984176A-12GENIChomozygous61065950
1205985266205985267AT24GENIChomozygous61065951
1206004902206004903TG8GENIChomozygous61065956
1206007330206007331GT24GENIChomozygous61065958
1206009313206009314TA7GENIChomozygous61065959
1206009666206009667AG27GENIChomozygous61065960
1206009701206009702AG15GENICpossibly homozygous61065961
1206010477206010478TC14GENIChomozygous61065962
1206012558206012559CT18GENIChomozygous61065963
1206012573206012579CTCCTG------4GENIChomozygous61065964