chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185608839156088392GA11GENIChomozygous110542874
185608919356089194AG7GENIChomozygous110361043
185609015856090159TC11GENIChomozygous110361045
185609156856091569CT14GENIChomozygous110361049
185609179656091797TC14GENIChomozygous110361051
185609277656092777CT7GENIChomozygous110361053
185609451456094515CA14GENIChomozygous110361057
185609467256094673AG8GENIChomozygous110361060
185609690756096908TC7GENIChomozygous110361066
185609746856097469AG16GENIChomozygous110361068
185609755656097557AG4GENIChomozygous125390778
185609843756098438AG6GENIChomozygous110361070
185609932156099322GT7GENIChomozygous110361072
185609952256099523GA18GENIChomozygous110361074
185610011456100115GT11GENIChomozygous119495632
185610169656101697GA21GENIChomozygous110542878
185610323856103239GA20GENIChomozygous110361076
185610332856103329GA17GENIChomozygous110361078
185610419156104192AG8GENIChomozygous110361080
185610515156105152GA13GENIChomozygous110542880
185610572256105723AG11GENIChomozygous110361082
185610647356106474TC9GENIChomozygous110361084
185610858456108585TC14GENIChomozygous110361088
185610913656109137GA14GENIChomozygous110361090
185610931656109317CT13GENIChomozygous110542882
185611268956112690AC9GENIChomozygous110361094
185611303456113035AG11GENICheterozygous119533698
185611332056113321AC16GENIChomozygous110542884
185611351156113512CA18GENIChomozygous125353020
185611358256113583TC9GENIChomozygous110542886
185611359456113595TC10GENIChomozygous125353021
185611440156114402TA8GENICheterozygous110542888