chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121206086121206087TC24GENIChomozygous54508531
7121206587121206588T-27GENIChomozygous56170108
7121207014121207015TG38GENIChomozygous54508533
7121207025121207026GA36GENIChomozygous56170110
7121207599121207600AG24GENIChomozygous56170112
7121208112121208113AG16GENIChomozygous56170114
7121208582121208583AG30GENIChomozygous54085695
7121209674121209675TG27GENICpossibly homozygous54508535
7121210449121210451AG--11GENICpossibly homozygous56170116
7121211375121211376TTAC28GENIChomozygous54085698
7121211559121211560AG23GENIChomozygous54508537
7121211999121212000AG25GENIChomozygous54508539
7121213364121213365CT25GENIChomozygous54085700
7121214678121214679GA34GENIChomozygous55585694
7121215288121215289TTACACAC4GENICheterozygous55631880
7121215288121215289TTACACACAC4GENICheterozygous55631882
7121216140121216141AG24GENIChomozygous54085702
7121217268121217269AG16GENIChomozygous54085703
7121217677121217678AC22GENIChomozygous54085705
7121218612121218613GGACAGAC11GENIChomozygous55002193
7121218795121218799GCCT----13GENIChomozygous55470073
7121219076121219077AT20GENIChomozygous54085711
7121219844121219846AC--6GENIChomozygous54085713
7121219944121219945TTC20GENIChomozygous56170118
7121221331121221332T-23GENIChomozygous54085714
7121221649121221650AG30GENIChomozygous54085716
7121222086121222087GGTCTC1GENIChomozygous56170120