chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105545725955457260CCACAG32GENIChomozygous51889925
105545735555457356TG54GENIChomozygous51459596
105545812755458128GC36GENIChomozygous51459597
105546044455460445GGTTT4GENIChomozygous51459598
105546044555460446GGT4GENIChomozygous51459600
105546046555460466CCG5GENIChomozygous51459601
105546047655460477CG8GENIChomozygous51459602
105546049655460497AG10GENIChomozygous51459603
105546049955460500AG10GENIChomozygous51459604
105546293155462932TC49GENIChomozygous51459605
105546660155466602GA23GENICheterozygous52158989
105546660955466613AGAG----6GENICheterozygous51459607
105546661155466613AG--6GENICheterozygous51459608
105546683655466837CCTTTTTTTT6GENIChomozygous51459609
105546685355466855GG--10GENICheterozygous51459610
105546724755467248GGAGACTCAAGGA16GENIChomozygous51459611
105546892555468926AT27GENIChomozygous51459612
105547094255470944AA--11GENIChomozygous51459614
105547250455472505GA26GENIChomozygous51459617
105547324355473247TATC----22GENIChomozygous51889940
105547325155473252TC26GENICheterozygous52158990
105547325255473256ATCC----15GENICheterozygous51459619
105547352755473528TC18GENIChomozygous51459621
105547435455474355TG21GENICpossibly homozygous51459622
105547435455474355TTTG14GENICheterozygous51459623
105547454755474551ATAC----10GENIChomozygous51652951
105547474655474747AAGT16GENIChomozygous52158991
105547528755475288AAC15GENICpossibly homozygous51459624
105547530655475307A-16GENICheterozygous51652957
105547591055475911TC21GENIChomozygous51459625
105547661155476612GA30GENIChomozygous51459626
105547690855476911TTT---8GENICheterozygous51889946
105547690955476911TT--8GENICheterozygous51889949
105547788755477888GA38GENIChomozygous51889952