chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18510393385103934GA12GENIChomozygous120482923
18510456685104567CG35GENIChomozygous120482924
18510461685104617GA36GENICpossibly homozygous120482925
18510521785105218GC23GENIChomozygous108881661
18510527185105272AT33GENIChomozygous108881662
18510575285105753AG45GENIChomozygous108881663
18510712985107130CA36GENIChomozygous120482926
18510760585107606GC26GENIChomozygous108881667
18510832185108322AG43GENIChomozygous120482927
18510947385109474CG36GENIChomozygous108881668
18511150185111502AG24GENICpossibly homozygous108881669
18511186585111866TC27GENIChomozygous108881670