chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130842583130842583AG56GENIChomozygous137983961
7130843191130843192TC63GENIChomozygous138224635
7130844214130844214G42GENIChomozygous137983962
7130845324130845325GA73GENIChomozygous138224636
7130847118130847119TC46GENIChomozygous138224637
7130847229130847230CT51GENIChomozygous138224638
7130847755130847756AG45GENIChomozygous138224639
7130847776130847777AC35GENICheterozygous403227303
7130846149130846150T23GENICheterozygous403227300
7130846149130846150TA23GENICheterozygous403227301
7130847776130847777A35GENICpossibly homozygous403227302
7130847777130847778A35GENICpossibly homozygous403227304
7130847777130847778AC35GENICheterozygous403227305
7130847778130847779A35GENICpossibly homozygous403227306
7130847778130847779AC35GENICheterozygous403227307
7130848030130848031CT68GENIChomozygous138224640
7130848222130848222AC73GENIChomozygous137983963
7130848655130848656GA56GENIChomozygous138224641
7130848794130848795CG57GENIChomozygous138224642