chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205960328205960329G-9GENIChomozygous61065912
1205960336205960339TTG---10GENICheterozygous61065913
1205960591205960592TC11GENIChomozygous62236344
1205960593205960595TC--11GENIChomozygous62030731
1205961237205961238CCT10GENIChomozygous61065916
1205961528205961529CT20GENIChomozygous61065917
1205962491205962492AG20GENIChomozygous61065918
1205963051205963052TC16GENIChomozygous61065919
1205963384205963385GGA8GENIChomozygous61065921
1205963592205963594AA--7GENIChomozygous61065922
1205963919205963920TC12GENIChomozygous61065924
1205964282205964283G-13GENIChomozygous61065925
1205964510205964511AG20GENIChomozygous61065928
1205965596205965597GT11GENIChomozygous61921321
1205966871205966872CT19GENIChomozygous62030732
1205966908205966909GA18GENIChomozygous61065931
1205967626205967630AAAT----10GENIChomozygous61065933
1205969956205969957GT9GENIChomozygous61065943
1205979294205979295TC15GENIChomozygous61065945
1205980171205980172GA18GENIChomozygous61065947
1205980247205980248GT24GENIChomozygous61065948
1205982040205982042TA--12GENIChomozygous61065949
1205982130205982131CT12GENIChomozygous62030735
1205985266205985267AT11GENIChomozygous61065951
1206004902206004903TG18GENIChomozygous61065956
1206006471206006480CTATAGTTT---------12GENIChomozygous62030740
1206007330206007331GT16GENIChomozygous61065958
1206008381206008382AG20GENIChomozygous62030741
1206009313206009314TA11GENIChomozygous61065959
1206009701206009702AG14GENIChomozygous61065961
1206011449206011450AT10GENIChomozygous62030743
1206011920206011927ACCCCCC-------9GENIChomozygous62030744
1206011940206011941CT11GENIChomozygous62030745
1206012558206012559CT8GENIChomozygous61065963