chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73661136636611367TC21GENIChomozygous886600418
73661191036611911AG26GENIChomozygous886600419
73661386536613866CT14GENIChomozygous886600420
73661409836614099GT3GENICheterozygous886600421
73661486636614867TC22GENIChomozygous886600422
73661559636615597GT4GENICheterozygous886600423
73661560136615602GT4GENICheterozygous886600424
73661894736618948CA10GENIChomozygous886600425
73662064036620641GA29GENIChomozygous886600426
73662140836621409AG24GENIChomozygous886600427
73662144436621445CT6GENIChomozygous886600428
73662236036622361GC29GENIChomozygous886600429
73662261936622620CT17GENIChomozygous886600430
73662355236623553CT9GENIChomozygous886600431
73662371936623720TC18GENIChomozygous886600432
73662431036624311TG19GENIChomozygous886600433
73662527536625276TG16GENIChomozygous886600434
73662544836625449CA14GENIChomozygous886600435
73662637036626371GT13GENIChomozygous886600436
73662743336627434AG7GENICheterozygous886600437
73662757536627576GC18GENIChomozygous886600438
73662835036628351TC8GENICheterozygous886600439
73662836336628364CT8GENICheterozygous886600440
73662978336629784CT12GENIChomozygous886600441
73663133136631332GT5GENIChomozygous886600442