chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
157535328775353288CCA8GENICpossibly homozygous768360999
157535329175353292TA10GENICpossibly homozygous669160242
157535353275353533CT11GENICpossibly homozygous669160243
157535388275353883AG11GENIChomozygous669160244
157535409475354095GA22GENIChomozygous669160245
157535439475354395CCG11GENICpossibly homozygous768361000
157535448875354489GC14GENICpossibly homozygous669160246
157535682075356821AG17GENICpossibly homozygous669160247
157535686075356861AG20GENIChomozygous669160248
157535842675358427TTGG2GENIChomozygous768361002
157535864175358642GA18GENIChomozygous669160249
157535865975358660GT21GENICpossibly homozygous669160250
157535887375358874CT20GENIChomozygous669160251
157535898875358989CT16GENICheterozygous669160252
157535917475359175TC1GENIChomozygous669160253
157535926475359265GA6GENIChomozygous669160254