chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130842583130842583AG22GENIChomozygous137983961
7130843191130843192TC23GENIChomozygous138224635
7130844214130844214G16GENIChomozygous137983962
7130845324130845325GA22GENIChomozygous138224636
7130846864130846864GC6GENICheterozygous145181901
7130847118130847119TC22GENIChomozygous138224637
7130847229130847230CT30GENIChomozygous138224638
7130847755130847756AG16GENIChomozygous138224639
7130847777130847778AC18GENICheterozygous403227305
7130846149130846150T18GENICheterozygous403227300
7130846149130846150TA18GENICheterozygous403227301
7130847776130847777A18GENIChomozygous403227302
7130847776130847777AC18GENICheterozygous403227303
7130847777130847778A18GENIChomozygous403227304
7130847778130847779A18GENIChomozygous403227306
7130847778130847779AC18GENICheterozygous403227307
7130848030130848031CT27GENIChomozygous138224640
7130848222130848222AC27GENIChomozygous137983963
7130848655130848656GA20GENIChomozygous138224641
7130848794130848795CG19GENIChomozygous138224642