chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121206086121206087TC12GENIChomozygous54508531
7121206587121206588T-17GENIChomozygous56170108
7121207014121207015TG32GENIChomozygous54508533
7121207025121207026GA32GENIChomozygous56170110
7121207599121207600AG22GENIChomozygous56170112
7121208112121208113AG16GENIChomozygous56170114
7121208582121208583AG19GENIChomozygous54085695
7121209674121209675TG13GENIChomozygous54508535
7121210449121210451AG--12GENIChomozygous56170116
7121211375121211376TTAC29GENIChomozygous54085698
7121211559121211560AG29GENIChomozygous54508537
7121211999121212000AG21GENIChomozygous54508539
7121213364121213365CT22GENIChomozygous54085700
7121214678121214679GA21GENIChomozygous55585694
7121215288121215289TTACACAC6GENICheterozygous55631880
7121215288121215289TTACACACAC6GENICheterozygous55631882
7121216140121216141AG24GENIChomozygous54085702
7121217268121217269AG22GENIChomozygous54085703
7121217677121217678AC16GENIChomozygous54085705
7121218612121218613GGACAGAC6GENIChomozygous55002193
7121218795121218799GCCT----10GENIChomozygous55470073
7121219076121219077AT20GENIChomozygous54085711
7121219379121219383ATAC----4GENICheterozygous56196899
7121219844121219846AC--10GENIChomozygous54085713
7121219944121219945TTC9GENIChomozygous56170118
7121221649121221650AG8GENIChomozygous54085716