chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125039128650391287TC36GENIChomozygous115352147
125039186250391863CT40GENIChomozygous115352149
125039204050392041AG54GENIChomozygous115352151
125039282050392821TA72GENICheterozygous115567826
125039383550393836CT37GENIChomozygous115352153
125039446250394463TG32GENIChomozygous115352155
125039470150394702TC46GENIChomozygous115352157
125039533050395331AG29GENIChomozygous115352159
125039607050396071GA55GENIChomozygous115352161
125039734150397342AG46GENIChomozygous115352163
125039777150397772GT71GENICpossibly homozygous115352165
125039783750397838GA63GENICpossibly homozygous115352167
125039836550398366AG67GENIChomozygous115352169
125039853450398535TA65GENIChomozygous115352171
125039862050398621GA124GENICheterozygous118274610
125039863950398640GT120GENICheterozygous118274611
125039864050398641CT119GENICheterozygous118274612
125039866050398661AG100GENICheterozygous118274613
125039869850398699CT59GENIChomozygous115403546
125039883050398831GA43GENIChomozygous115403548
125039902550399026CT36GENICpossibly homozygous115352173
125039918350399184AG61GENIChomozygous115352175
125039937250399373CT54GENIChomozygous115352177
125039943650399437CT60GENICpossibly homozygous115352179
125039968550399686GA61GENIChomozygous115352181
125040057050400571AT41GENIChomozygous115352183
125040060250400603AG29GENIChomozygous115352185
125040126050401261GA51GENICpossibly homozygous115352187
125040127650401277CT43GENIChomozygous115352189
125040173250401733CT53GENIChomozygous115352191
125040195050401951AG55GENIChomozygous115352193
125040202550402026GA49GENIChomozygous115352195
125040364550403646TC40GENIChomozygous115352197
125040427850404279GA51GENIChomozygous115352199
125040431650404317CT54GENIChomozygous115352201
125040441350404414TC55GENICpossibly homozygous115352203