chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105685174156851742AT38GENIChomozygous116935793
105685182756851828CA34GENIChomozygous117059972
105685214156852142GA29GENIChomozygous116935795
105685215856852159TC33GENIChomozygous116978107
105685230856852309GC52GENIChomozygous116935797
105685259956852600GA60GENIChomozygous116935799
105685320356853204TC39GENIChomozygous116935803
105685324156853242GA32GENIChomozygous116935805
105685414856854149GA43GENIChomozygous116935807
105685498056854981AT43GENIChomozygous116935809
105685520756855208AG45GENIChomozygous116935811
105685567756855678GC52GENIChomozygous116935813
105685302556853026TG49GENIChomozygous116784373
105685317256853173TG39GENIChomozygous116784375
105685596856855969AG46GENIChomozygous116784381
105685620356856204GA54GENIChomozygous116935815
105685663356856634TC35GENIChomozygous116935817
105685695456856955AG40GENIChomozygous116935823
105685732856857329TG48GENIChomozygous116935827
105685758156857582AG54GENIChomozygous116784389
105685780756857808GA50GENIChomozygous117059974
105685846856858469AG43GENIChomozygous116784391
105685881456858815CT48GENIChomozygous116935829
105685958056859581TC38GENIChomozygous116784393
105686033756860338CT52GENIChomozygous116935831
105686225856862259TA49GENIChomozygous116784397
105686320056863201AG31GENIChomozygous116978109
105686354756863548TC40GENIChomozygous117059976
105686357856863579AG39GENIChomozygous116784401
105686358556863586CT40GENIChomozygous117059978
105685347956853479A38GENICpossibly homozygous131094613
105685350156853502T41GENIChomozygous131094614