chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4179045987179045988CA9GENIChomozygous80489226
4179045996179045997TC6GENIChomozygous80489228
4179045997179045998TC6GENIChomozygous80489230
4179050823179050824CA10GENIChomozygous71322018
4179060560179060561TC18GENICheterozygous71322024
4179063960179063961CT14GENIChomozygous73343081
4179046504179046505CT26GENIChomozygous73343075
4179061278179061279GA20GENIChomozygous73343078
4179061830179061831TA29GENIChomozygous73343079
4179062018179062019CT39GENIChomozygous73343080
4179064523179064524TC22GENIChomozygous73343082
4179076438179076439GA27GENICheterozygous71322030
4179085488179085489TC20GENIChomozygous71322062
4179086115179086116AG22GENIChomozygous71322070
4179086782179086783CT29GENIChomozygous73343084
4179089535179089536AG25GENIChomozygous71322080
4179091720179091721GA19GENIChomozygous73343085
4179096274179096275GA28GENIChomozygous73343088
4179100827179100828TC21GENICpossibly homozygous71322122
4179103316179103317AT4GENIChomozygous80394199
4179104146179104147GA19GENIChomozygous73343089
4179110878179110879AT11GENIChomozygous71322136
4179115023179115024GT20GENIChomozygous73343091