chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4148082102148082103G-1GENIChomozygous56974355
4148082113148082114A-1GENIChomozygous56974356
4148082129148082130AT6GENIChomozygous56974357
4148118858148118859A-3GENICheterozygous57837534
4148156474148156475AAT1GENIChomozygous56974454
4148176385148176386CCCT20GENICpossibly homozygous56974458
4148193527148193528CCA1GENIChomozygous56974495
4148193535148193536CCA2GENIChomozygous56974496
4148195809148195810T-2GENICheterozygous57347963
4148212693148212694C-16GENICheterozygous56974507
4148228958148228959AT8GENICpossibly homozygous56974527
4148280513148280514CCT4GENICheterozygous57348140
4148280514148280515T-4GENICheterozygous58085083
4148280939148280940GT21GENICpossibly homozygous56974667
4148283438148283439T-2GENICheterozygous56974673
4148297574148297575G-5GENIChomozygous56974708
4148297585148297586TC5GENIChomozygous56974709
4148297592148297593CA4GENIChomozygous56974710
4148297599148297600C-1GENIChomozygous56974711
4148299896148299897TTAC2GENICheterozygous57348167
4148308820148308822TC--7GENICheterozygous57348179
4148331074148331075AG1GENIChomozygous56974772
4148334093148334094CA18GENICpossibly homozygous58703730
4148334105148334106AT11GENIChomozygous58703733
4148348720148348721CT16GENICheterozygous56974841
4148381001148381002T-1GENIChomozygous56975022
4148384109148384110C-17GENICpossibly homozygous56975040
4148387388148387389CCAGAG2GENICheterozygous58345428
4148388645148388646AC4GENICheterozygous56975061
4148445237148445238A-1GENIChomozygous57951963
4148462565148462567AT--3GENICheterozygous56975245
4148497900148497901A-6GENICheterozygous58703735