chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166459078166459079GA23GENIChomozygous109342425
1166462164166462165CG27GENIChomozygous108356487
1166462553166462554GA29GENIChomozygous108954833
1166464640166464641CT40GENIChomozygous108356488
1166486354166486355CG38GENIChomozygous108356499
1166508457166508458AG39GENIChomozygous108356518
1166509324166509325AG31GENIChomozygous108356519
1166509471166509472GT31GENIChomozygous108356521
1166509943166509944AG31GENIChomozygous109342427
1166510137166510138CT29GENIChomozygous108356522
1166511134166511135TC27GENIChomozygous108954882
1166511155166511156AT24GENIChomozygous108954883
1166511176166511177GA26GENIChomozygous108954884
1166511209166511210AG28GENIChomozygous108954885
1166513164166513165TC31GENIChomozygous108356524
1166515244166515245AG24GENIChomozygous108954886
1166516391166516392GT22GENIChomozygous108954887
1166516438166516439AG32GENIChomozygous108954888
1166516609166516610TC39GENIChomozygous108954889
1166516895166516896AG35GENIChomozygous109342429
1166517106166517107GA25GENIChomozygous108954891
1166517487166517488TC18GENIChomozygous108954892
1166517728166517729AC35GENIChomozygous108954893
1166518877166518878AG24GENIChomozygous108356527
1166518999166519000GA43GENICpossibly homozygous109342431
1166519109166519110GA51GENICpossibly homozygous109342433
1166519366166519367AC30GENIChomozygous108356528
1166519468166519469GA39GENIChomozygous108954894
1166519583166519584TC31GENIChomozygous108954895
1166519687166519688CT29GENIChomozygous108954896
1166519757166519758TA32GENIChomozygous108356529
1166522243166522244CT40GENIChomozygous108954897
1166522760166522761AG46GENIChomozygous108356531
1166523106166523107AG19GENIChomozygous108954898
1166523166166523167TC21GENIChomozygous108356532
1166523969166523970GA27GENIChomozygous108356534