chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186295790162957902A10GENIChomozygous130473111
186295791762957917A13GENIChomozygous129544812
186295792662957927TA14GENIChomozygous119497714
186295795162957951C14GENIChomozygous129544813
186295795862957959A14GENIChomozygous129544814
186295796062957960GA14GENIChomozygous129544815
186295798362957983AG15GENIChomozygous129544816
186295812962958129A4GENIChomozygous130473112
186295848462958484C14GENIChomozygous129544817
186295860862958608C43GENIChomozygous129544818
186295865462958655T47GENIChomozygous129544819
186295866262958663C46GENIChomozygous129544820
186295867062958671T48GENIChomozygous129544821
186295877062958771CA45GENIChomozygous110634141
186295881662958817G37GENIChomozygous129544822
186295885162958852G37GENIChomozygous129544824
186295885562958855C36GENIChomozygous129544825
186295886362958864C35GENIChomozygous129544826
186295887162958872T36GENIChomozygous129544827
186295889462958895A39GENIChomozygous129544828
186295889962958900T40GENIChomozygous129544829
186295890362958904A40GENIChomozygous129544830
186295895362958954CA40GENIChomozygous110379261
186295896062958961G40GENIChomozygous129544831
186295896362958963G40GENIChomozygous129544832
186295896462958965GA41GENIChomozygous110379263
186295898962958990T40GENIChomozygous129544833
186295900962959010T40GENIChomozygous129544834
186295904362959044T42GENIChomozygous129544836
186295903462959035T42GENIChomozygous129544835
186295907662959077A37GENIChomozygous129544837
186295908562959086AC37GENIChomozygous110379265
186295908762959087G36GENIChomozygous129544838
186295992262959922T31GENIChomozygous129544839
186296439662964396T37GENIChomozygous129544842
186296441762964417C35GENIChomozygous130473113
186296442162964421T35GENIChomozygous129544844
186296443662964436T37GENIChomozygous129544845