chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1420211482021149AG41GENIChomozygous959088784
1420211762021177TC33GENIChomozygous959088785
1420224522022453AG17GENIChomozygous959088786
1420226232022624AG18GENIChomozygous959088787
1420234352023436CT31GENIChomozygous959088788
1420235412023542GA47GENIChomozygous959088789
1420238482023849AG28GENIChomozygous959088790
1420241392024140AG18GENIChomozygous959088791
1420241602024161AG21GENICpossibly homozygous959088792
1420244562024457CT34GENIChomozygous959088793
1420246722024673AG27GENIChomozygous959088794
1420258692025870TC32GENIChomozygous959088795
1420277952027796CT32GENIChomozygous959088796
1420278082027809TC32GENIChomozygous959088797
1420279222027923GC26GENICheterozygous959088798
1420284062028407GA33GENIChomozygous959088799
1420285162028517TC28GENIChomozygous959088800
1420301082030109CT18GENIChomozygous959088801
1420311392031140CT34GENIChomozygous959088802
1420311712031172TC36GENIChomozygous959088803