chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176969592869695929AT14GENIChomozygous809807975
176969781969697820GA32GENIChomozygous809807976
176969798469697985CT51GENIChomozygous809807977
176969870469698705TC46GENIChomozygous809807978
176969885769698858AG40GENIChomozygous809807979
176969939669699397GA25GENICpossibly homozygous809807980
176969940469699405TG26GENICpossibly homozygous809807981
176969950369699504AG21GENIChomozygous809807982
176970099469700995CT63GENICpossibly homozygous809807983
176970127169701272CT51GENIChomozygous809807984
176970155369701554GA58GENIChomozygous809807985
176970243469702435CA55GENICheterozygous809807986
176970294369702944TC39GENIChomozygous809807987
176970310469703105GC115GENICheterozygous809807988
176970316269703163GT83GENICheterozygous809807989
176970333869703339GT43GENIChomozygous809807990
176970353769703538GT156GENICheterozygous809807991
176970361069703611AT197GENICheterozygous809807992
176970362969703630GC224GENICheterozygous809807993
176970450469704505GA56GENIChomozygous809807994
176970917969709180TC45GENIChomozygous809807995
176971133369711334TG43GENICpossibly homozygous809807996