chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4222553156222553157CCTT17GENIChomozygous57103296
4222553189222553190TC16GENIChomozygous57103297
4222553629222553630G-28GENIChomozygous57103298
4222553865222553866CT34GENIChomozygous57103299
4222553908222553909CT36GENIChomozygous57103300
4222553988222553989TTAGA20GENIChomozygous57103301
4222554174222554175AAT32GENICpossibly homozygous57103302
4222554562222554563GGA27GENIChomozygous57103303
4222554717222554718CCT22GENIChomozygous57103304
4222554912222554913GA38GENIChomozygous57103305
4222555123222555124CT13GENIChomozygous57103306
4222556626222556628TT--12GENICheterozygous57103307
4222556642222556643GGTTCT9GENICheterozygous58448170
4222556902222556903TTTGTTTTG24GENICheterozygous57103310
4222556946222556947CT29GENIChomozygous57103311
4222557261222557262TC26GENIChomozygous57103313
4222557760222557761TC23GENIChomozygous57103314
4222558307222558308TTA27GENIChomozygous57103315
4222559522222559523AATT16GENIChomozygous57103316
4222559746222559752TTTTGT------17GENIChomozygous57103317
4222560144222560145CCT10GENIChomozygous57103318
4222556642222556643GGTTT9GENICpossibly homozygous58375540
4222558308222558309TA27GENIChomozygous57368161