chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3165713655165713656CG21GENIChomozygous111809951
3165714296165714297TC15GENIChomozygous112432447
3165716419165716420GA29GENIChomozygous111809954
3165716460165716461AG23GENIChomozygous111809956
3165716510165716511GT10GENIChomozygous111809958
3165716853165716854AG22GENIChomozygous111809961
3165717505165717506GA15GENIChomozygous111809963
3165718421165718422AT14GENIChomozygous111809965
3165718770165718771TC15GENIChomozygous111809968
3165719864165719865CT19GENIChomozygous111809970
3165720755165720756TC27GENIChomozygous111809973
3165721697165721698CT5GENICheterozygous119705460
3165721705165721706TC4GENIChomozygous119705461
3165721722165721723AG4GENIChomozygous119880592
3165723500165723501AG13GENIChomozygous111809977
3165724937165724938CG15GENIChomozygous111809979
3165725110165725111AG14GENIChomozygous111809982
3165725159165725160AG12GENIChomozygous111809984
3165725666165725667CG16GENIChomozygous111809987
3165725787165725788GA21GENIChomozygous111809989
3165727365165727366TC25GENIChomozygous111810003
3165730403165730404GA14GENIChomozygous111810010
3165730805165730806CT23GENIChomozygous111810012
3165732815165732816TC13GENIChomozygous111810017
3165733239165733240AG30GENIChomozygous111810019
3165733902165733903AG21GENIChomozygous111810022
3165734051165734052CT17GENIChomozygous111810024
3165734529165734530GA18GENIChomozygous111810027
3165734668165734669AG28GENIChomozygous111810029
3165734746165734747AG34GENIChomozygous111810032
3165734887165734888GA31GENIChomozygous111810034
3165735012165735013CG22GENIChomozygous111810036
3165736652165736653GA16GENIChomozygous111810039
3165738866165738867TC18GENIChomozygous111810041
3165740269165740270CT10GENIChomozygous111810043
3165740601165740602CT17GENIChomozygous111810046
3165740912165740913GA12GENIChomozygous111810048
3165741893165741894GA13GENIChomozygous111810051