chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103657968103657969AG29GENIChomozygous521099471
10103658439103658440AG46GENIChomozygous521099472
10103659619103659620TG42GENIChomozygous523781540
10103659887103659889CC--10GENICheterozygous691142404
10103659899103659900G-15GENICheterozygous691142406
10103662173103662174AC36GENIChomozygous523781541
10103662211103662212GGA27GENIChomozygous691142407
10103662344103662345CA25GENICheterozygous523781542
10103662594103662595AG50GENICpossibly homozygous523781543
10103662601103662602CCT28GENICheterozygous691142408
10103662715103662719TTTT----15GENIChomozygous691142409
10103664257103664258CT46GENIChomozygous523781544
10103664985103664986CT26GENICheterozygous523781545
10103665312103665313CT31GENIChomozygous523781546
10103665617103665618CT33GENIChomozygous523781547
10103665767103665768AG22GENIChomozygous521099473
10103665802103665803CT20GENIChomozygous523781548
10103667631103667632CT48GENIChomozygous523781549
10103667793103667794AG37GENICpossibly homozygous521099474
10103667854103667855AG33GENIChomozygous521099475
10103668540103668541CCAA14GENIChomozygous691142410
10103669357103669358GA34GENICpossibly homozygous523781550
10103669648103669649AG28GENIChomozygous523781551
10103669968103669969CT42GENICpossibly homozygous521099476
10103670093103670094AT31GENIChomozygous523781552
10103670167103670168GA39GENIChomozygous523781553
10103670279103670280GA32GENIChomozygous523781554