chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105685174156851742AT28GENIChomozygous116935793
105685182756851828CA37GENIChomozygous117059972
105685214156852142GA30GENIChomozygous116935795
105685230856852309GC31GENIChomozygous116935797
105685259956852600GA34GENIChomozygous116935799
105685302556853026TG20GENIChomozygous116784373
105685317256853173TG29GENIChomozygous116784375
105685320356853204TC21GENIChomozygous116935803
105685324156853242GA18GENIChomozygous116935805
105685414856854149GA19GENIChomozygous116935807
105685498056854981AT28GENIChomozygous116935809
105685520756855208AG25GENICpossibly homozygous116935811
105685567756855678GC36GENIChomozygous116935813
105685596856855969AG28GENIChomozygous116784381
105685620356856204GA33GENIChomozygous116935815
105685663356856634TC25GENIChomozygous116935817
105685695456856955AG23GENIChomozygous116935823
105685732856857329TG22GENIChomozygous116935827
105685758156857582AG23GENIChomozygous116784389
105685780756857808GA21GENIChomozygous117059974
105685846856858469AG38GENIChomozygous116784391
105685881456858815CT33GENIChomozygous116935829
105685958056859581TC21GENIChomozygous116784393
105686033756860338CT33GENIChomozygous116935831
105686225856862259TA32GENIChomozygous116784397
105686320056863201AG16GENIChomozygous116978109
105686354756863548TC22GENIChomozygous117059976
105686357856863579AG23GENIChomozygous116784401