chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47828344078283441CT26GENIChomozygous113125217
47828374078283741CT34GENICpossibly homozygous113125218
47828576078285761GC32GENIChomozygous113125219
47828631878286319TC34GENIChomozygous113125220
47828652878286529GA25GENICpossibly homozygous113125221
47828767578287676CT30GENIChomozygous113125222
47828866478288665TC44GENIChomozygous113125223
47828880078288801AG24GENIChomozygous113125224
47828908878289089TC8GENIChomozygous113125225
47828955178289552AC19GENIChomozygous113125226
47828973778289738TC18GENIChomozygous113125227
47828979878289799TG23GENIChomozygous113125228
47829010678290107CT24GENIChomozygous113125229
47829018278290183TA22GENIChomozygous113125230
47829051078290511CG26GENIChomozygous113125231
47829090378290904TA38GENIChomozygous113125232
47829250678292507AG15GENIChomozygous113125233
47829316678293167AG44GENIChomozygous113125234
47829364978293650CA27GENIChomozygous113125236
47829403478294035GA24GENIChomozygous113125237