chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242322324232233TC18GENIChomozygous530366030
1242327264232727AG29GENIChomozygous530366031
1242328904232891TTCCCTCC9GENIChomozygous694486392
1242336644233670GTGTGT------7GENICpossibly homozygous694486394
1242338354233836GC18GENIChomozygous530366032
1242338884233889GA16GENIChomozygous530366033
1242340884234089TC20GENIChomozygous530366034
1242343054234306TC19GENIChomozygous530366035
1242344524234453TC19GENIChomozygous530366036
1242346594234660A-17GENICpossibly homozygous694486395
1242346604234665AACAC-----19GENICheterozygous694486396
1242348524234867AAAAAAAGAAAGAAA---------------5GENICheterozygous694486397
1242350874235088TG26GENIChomozygous530366037
1242355454235546GC25GENICpossibly homozygous530366038
1242358524235853CA19GENIChomozygous530366039
1242359274235928TC29GENICpossibly homozygous530366040
1242359854235986TC29GENICpossibly homozygous530366041
1242373164237317GT17GENIChomozygous530366042
1242374124237413TTGGTTATTCAACTCGACCTTTGAA10GENIChomozygous694486398
1242374454237446AAT26GENIChomozygous694486399
1242374524237453GA28GENIChomozygous530366043
1242396454239646TA25GENIChomozygous530366044
1242401504240151CCT24GENIChomozygous694486400
1242415534241557GTGT----4GENIChomozygous694486401
1242430874243091GTGT----13GENIChomozygous694486403
1242440344244035TTTC9GENICheterozygous694486404
1242440824244083AAGTGTGT3GENIChomozygous694486405
1242454294245430GGAC23GENIChomozygous694486408
1242455704245571TTAC36GENIChomozygous694486409
1242484834248484CA5GENIChomozygous530366045
1242491914249193AA--17GENICheterozygous694486410
1242519794251980AG30GENIChomozygous530366046
1242541964254197AG27GENICpossibly homozygous531943761
1242547054254709TACA----15GENIChomozygous694486412
1242586264258627CT21GENIChomozygous531943762