chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34180945041809452CT7GENICheterozygous136558173
34183101441831015TG26GENIChomozygous140989657
34187999541879996GT31GENICheterozygous403062135
34190399041903991AT10GENICheterozygous154099375
34187999541879996G31GENICpossibly homozygous403062136
34190399041903991A10GENICheterozygous403062137
34190314441903145T5GENIChomozygous404411683
34190314441903145TC5GENICheterozygous404411684
34190314641903147T5GENIChomozygous404411685
34190314641903147TC5GENICheterozygous404411686
34191959541919596T17GENICheterozygous403062138
34191959541919596TC17GENICheterozygous403062139
34191961741919618TG17GENICheterozygous136684031
34193453641934537AG6GENICheterozygous403062140