chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6144512102144512104TA--13GENIChomozygous760910775
6144512667144512668CT21GENIChomozygous656492197
6144512768144512769CT38GENIChomozygous656492198
6144513359144513360GT25GENICpossibly homozygous656492199
6144515727144515728AG50GENIChomozygous656492200
6144515833144515834TC41GENIChomozygous656492201
6144516170144516171AG27GENICpossibly homozygous656492202
6144518272144518273AT22GENIChomozygous656492203
6144518417144518418CCG29GENIChomozygous760910776
6144518550144518551CT44GENICpossibly homozygous656492204
6144518607144518608GT46GENIChomozygous656492205
6144518869144518870CA38GENIChomozygous656492206
6144518987144518988TA33GENICpossibly homozygous656492207
6144519638144519639GA32GENIChomozygous656492208
6144520045144520046AT26GENIChomozygous656492209
6144520151144520152TC37GENIChomozygous656492210
6144520883144520884CCA29GENIChomozygous760910777
6144520887144520888CCT31GENIChomozygous760910778
6144521666144521667GA26GENIChomozygous656492211
6144522103144522104AG29GENIChomozygous656492212
6144523159144523160TTGGA7GENIChomozygous760910780
6144523383144523384TC23GENIChomozygous656492213
6144523524144523525CT26GENIChomozygous656492214
6144523689144523690C-20GENIChomozygous760910781
6144524668144524669AG24GENIChomozygous656492215