chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5137675697137675698CT5GENICheterozygous55745514
5137675827137675874GATGGTGACCTCTGGACTCAGGGAGCCCCAGCATCCATAGCACAGGT-----------------------------------------------2GENICheterozygous56354900
5137676449137676452GTG---13GENICheterozygous55745520
5137677515137677516TC7GENIChomozygous55745521
5137677728137677729CT21GENICpossibly homozygous55745522
5137678231137678232GT18GENIChomozygous55745523
5137680439137680440CG20GENIChomozygous55745528
5137684491137684492AG15GENICpossibly homozygous55745529
5137685416137685417AACACAC2GENIChomozygous55745530
5137685584137685585GA20GENIChomozygous55745532
5137688816137688817TA24GENICpossibly homozygous55745534