chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122394148923941490GA27GENIChomozygous115286191
122394272823942729CG30GENIChomozygous115286193
122394294723942948CT34GENIChomozygous115286195
122394326923943270GA19GENIChomozygous115469773
122394368323943684TG39GENIChomozygous115286197
122394467123944672AG15GENIChomozygous115469775
122394483523944836TG36GENIChomozygous115286199
122394507723945078TC34GENIChomozygous115286201
122394561423945615TC23GENIChomozygous115286205
122394591423945915CT23GENIChomozygous115286207
122394626623946267AG29GENIChomozygous115286209
122394656023946561CT33GENIChomozygous115286213
122394657423946575TA18GENIChomozygous115438578
122394665223946653CG22GENIChomozygous115469777
122394680223946803GA27GENIChomozygous115422064
122394779023947791AC24GENIChomozygous115286215
122394791623947917CA30GENIChomozygous115286217
122394818623948187TA22GENIChomozygous115286219
122394872823948729CA31GENIChomozygous115286221
122394883223948833TC25GENIChomozygous115286223
122394929523949296TA34GENIChomozygous115286227
122394983323949834AT29GENIChomozygous115286229
122395033923950340CT27GENIChomozygous115286233
122395120423951205AG32GENIChomozygous115286235
122395131823951319GA37GENIChomozygous115286237
122395148123951482CT36GENIChomozygous115438584
122395182323951824CT30GENIChomozygous115286239