chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117521242775212428TTCC9GENICpossibly homozygous51169693
117521330075213301AG25GENIChomozygous50962842
117521388275213883GA15GENIChomozygous50962843
117521455975214560CT14GENIChomozygous50962844
117521857875218579AAT13GENICheterozygous50962845
117521857875218579AATT13GENICheterozygous50962846
117521948575219486AG20GENIChomozygous50962847
117522273975222740TC14GENIChomozygous50962848
117522429975224300TC20GENIChomozygous50962849
117522445375224454TC23GENIChomozygous50962850
117522539475225395TC22GENIChomozygous50962851
117522540075225401TA22GENIChomozygous50962852
117522540175225402AT22GENIChomozygous51169694
117522968775229688A-16GENIChomozygous50962853
117523002775230028AAT17GENICpossibly homozygous50962854
117523003775230038CT18GENIChomozygous50962855
117523081975230820GGAATA8GENIChomozygous50962857
117523118675231187GA21GENIChomozygous50962858
117522415475224160AAAAAC------4GENICheterozygous51221453
117522417375224181ACCAAACC--------5GENIChomozygous51221455
117522415575224160AAAAC-----4GENICheterozygous50892818