chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5176797107176797108TC24GENIChomozygous55849667
5176797794176797795TC38GENIChomozygous55849668
5176797975176797976TG25GENIChomozygous55849669
5176799637176799643ATATAT------24GENICheterozygous55949609
5176799639176799643ATAT----24GENICheterozygous56497442
5176799641176799643AT--24GENICheterozygous55849670
5176800136176800137T-14GENICpossibly homozygous55849671
5176801102176801103TTTTTG16GENIChomozygous55849672
5176801187176801188T-21GENIChomozygous55849673
5176801312176801314TT--26GENIChomozygous55849674
5176803572176803573CCTTTTTTTTTTT14GENIChomozygous56466785
5176803593176803594TG28GENIChomozygous55849678
5176805970176805971CCTTTTTTTTTTTTT3GENICheterozygous56533545
5176805974176805978TTTC----5GENICheterozygous56533546
5176806856176806857TTG11GENICheterozygous55849684
5176804795176804796CT44GENIChomozygous55849680
5176805155176805156TC30GENIChomozygous55849681
5176806371176806372T-15GENICpossibly homozygous55849682
5176807848176807849GA32GENIChomozygous55849685
5176808181176808182TC29GENIChomozygous55849686
5176808384176808387TTT---15GENICpossibly homozygous55849687
5176808385176808387TT--15GENICheterozygous56466789
5176808831176808832CT18GENIChomozygous55849688
5176808862176808863GGA14GENIChomozygous55849689
5176808874176808875CCAAAAAA6GENIChomozygous56466790
5176808936176808937AG20GENIChomozygous55849690
5176809122176809123TC35GENIChomozygous55849691
5176809223176809224GA23GENIChomozygous55849692
5176810518176810519CCTGCAGT26GENIChomozygous55849693