chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6137187453137187454GT11GENIChomozygous114996766
6137188005137188006CA16GENIChomozygous114996767
6137191526137191527GA23GENIChomozygous114996768
6137192078137192079GA22GENIChomozygous114996769
6137194520137194521TC20GENIChomozygous114996772
6137198427137198428CA17GENIChomozygous114996773
6137199866137199867CA16GENIChomozygous115228824
6137199924137199925CT19GENIChomozygous114996774
6137200089137200090TC26GENIChomozygous114996775
6137201444137201444A18GENIChomozygous128400635
6137193752137193752CC21GENIChomozygous128400632
6137199463137199463G19GENIChomozygous128400634
6137201448137201449A18GENIChomozygous128400636
6137201464137201465G12GENIChomozygous128400637
6137201470137201471TC12GENIChomozygous114996776
6137201486137201487GC13GENIChomozygous114996777
6137202218137202219AG19GENIChomozygous114996778
6137202464137202465AG20GENIChomozygous114996779
6137204401137204402CT27GENIChomozygous114996780
6137204504137204505AT30GENICpossibly homozygous114996781
6137204703137204704AG18GENIChomozygous114996782
6137205480137205481CT13GENIChomozygous114996783
6137205722137205722GCAT14GENIChomozygous128400638
6137206023137206024TC6GENIChomozygous114996784
6137206342137206343TC12GENIChomozygous114996785
6137201451137201452AG18GENIChomozygous118556407