chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130842583130842583AG53GENIChomozygous137983961
7130843191130843192TC55GENIChomozygous138224635
7130844214130844214G35GENICpossibly homozygous137983962
7130845324130845325GA67GENIChomozygous138224636
7130846149130846150T38GENICheterozygous403227300
7130846149130846150TA38GENICheterozygous403227301
7130847118130847119TC39GENIChomozygous138224637
7130847229130847230CT57GENIChomozygous138224638
7130847755130847756AG41GENIChomozygous138224639
7130847776130847777A26GENICheterozygous403227302
7130847776130847777AC26GENICheterozygous403227303
7130847777130847778A26GENICheterozygous403227304
7130847777130847778AC26GENICheterozygous403227305
7130847778130847779A26GENICheterozygous403227306
7130847778130847779AC26GENICheterozygous403227307
7130848030130848031CT75GENIChomozygous138224640
7130848222130848222AC71GENIChomozygous137983963
7130848655130848656GA65GENIChomozygous138224641
7130848794130848795CG68GENIChomozygous138224642