chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110470112110470113AG6GENIChomozygous117035953
10110470979110470980AG5GENIChomozygous116720734
10110471865110471866GA8GENIChomozygous116720736
10110474643110474644TC6GENIChomozygous116720738
10110474870110474871GA10GENIChomozygous116720740
10110475466110475467AG3GENIChomozygous116720742
10110476387110476388AG9GENIChomozygous116720744
10110477076110477077AG5GENIChomozygous116720746
10110477142110477143TA6GENIChomozygous116720748
10110478078110478079CT7GENIChomozygous116983874
10110480051110480052CT9GENIChomozygous116910206
10110481191110481192AG3GENIChomozygous116720754
10110482465110482466GA6GENIChomozygous116720756
10110483535110483536AG6GENIChomozygous116720758
10110483823110483824CT5GENIChomozygous116720760
10110484557110484558CG2GENIChomozygous116720762
10110484661110484662GA4GENIChomozygous116720764
10110486291110486292TA4GENIChomozygous116720772
10110485965110485966AG2GENIChomozygous116720770
10110487034110487035CA2GENIChomozygous116720774
10110488054110488055CT8GENIChomozygous116720776
10110488587110488588GA4GENIChomozygous116720778
10110489420110489421AG12GENIChomozygous116720780
10110489523110489524TC2GENIChomozygous116720782
10110490726110490727GA6GENIChomozygous116720784
10110493415110493416GT4GENIChomozygous116720786
10110495040110495041GA8GENIChomozygous116720788
10110497633110497634GA9GENIChomozygous116720790
10110497668110497669AG8GENIChomozygous116720792
10110498831110498832AG10GENIChomozygous116720794
10110498842110498843CT10GENIChomozygous116720796
10110500749110500750GT7GENIChomozygous116720798
10110505606110505607GT10GENIChomozygous116720800
10110505608110505609TC10GENIChomozygous116720802
10110510213110510214GA4GENIChomozygous116720804
10110511067110511068AG9GENIChomozygous116720806
10110513563110513564CA4GENIChomozygous116720808
10110514549110514550AT6GENIChomozygous116720810