chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4222553156222553157CCTT27GENIChomozygous57103296
4222553189222553190TC54GENIChomozygous57103297
4222553629222553630G-45GENIChomozygous57103298
4222553865222553866CT58GENIChomozygous57103299
4222553908222553909CT54GENIChomozygous57103300
4222553988222553989TTAGA51GENIChomozygous57103301
4222554174222554175AAT56GENIChomozygous57103302
4222554562222554563GGA51GENICpossibly homozygous57103303
4222554717222554718CCT59GENIChomozygous57103304
4222554912222554913GA78GENIChomozygous57103305
4222555123222555124CT37GENIChomozygous57103306
4222556626222556628TT--14GENICheterozygous57103307
4222556642222556643GGTTC20GENICheterozygous57103308
4222556902222556903TTTGTTTTG26GENIChomozygous57103310
4222556946222556947CT17GENICpossibly homozygous57103311
4222557127222557128A-3GENIChomozygous57103312
4222557261222557262TC53GENIChomozygous57103313
4222557760222557761TC50GENIChomozygous57103314
4222558307222558308TTA68GENIChomozygous57103315
4222559522222559523AATT39GENIChomozygous57103316
4222559746222559752TTTTGT------18GENIChomozygous57103317
4222560144222560145CCT19GENIChomozygous57103318
4222558308222558309TA74GENICpossibly homozygous57368161