chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166462164166462165CG24GENIChomozygous108356487
1166462177166462178CT26GENIChomozygous109436768
1166462553166462554GA21GENIChomozygous108954833
1166464640166464641CT24GENIChomozygous108356488
1166508457166508458AG24GENIChomozygous108356518
1166509324166509325AG19GENIChomozygous108356519
1166509471166509472GT32GENIChomozygous108356521
1166509910166509911AT30GENIChomozygous109163642
1166509911166509912TC30GENIChomozygous109163644
1166509943166509944AG24GENIChomozygous109342427
1166511134166511135TC27GENIChomozygous108954882
1166511155166511156AT30GENIChomozygous108954883
1166511176166511177GA30GENIChomozygous108954884
1166511209166511210AG26GENIChomozygous108954885
1166513164166513165TC35GENIChomozygous108356524
1166515244166515245AG27GENIChomozygous108954886
1166516438166516439AG28GENIChomozygous108954888
1166516609166516610TC14GENIChomozygous108954889
1166517106166517107GA32GENICpossibly homozygous108954891
1166517487166517488TC23GENIChomozygous108954892
1166517728166517729AC12GENIChomozygous108954893
1166518877166518878AG35GENIChomozygous108356527
1166519366166519367AC19GENIChomozygous108356528
1166519468166519469GA23GENIChomozygous108954894
1166519583166519584TC23GENIChomozygous108954895
1166519687166519688CT30GENIChomozygous108954896
1166519757166519758TA30GENIChomozygous108356529
1166522243166522244CT24GENIChomozygous108954897
1166522760166522761AG16GENIChomozygous108356531
1166523106166523107AG23GENIChomozygous108954898
1166523166166523167TC12GENIChomozygous108356532
1166523969166523970GA27GENIChomozygous108356534