chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5130892774130892775CG16GENICheterozygous55896480
5130892854130892855CA9GENICheterozygous55896481
5130897315130897316C-10GENICheterozygous55720312
5130898083130898084AG10GENICheterozygous55720322
5130899554130899555GA32GENICheterozygous55720328
5130915047130915048TC18GENICheterozygous55720356
5130917801130917802CT75GENICheterozygous56814995
5130959716130959717G-31GENICheterozygous55720520
5131015673131015674CA16GENICheterozygous56563170
5131015674131015675AC16GENICheterozygous56563171
5131015682131015683TG22GENICheterozygous55720816
5131015914131015915GA11GENICheterozygous55720818
5131044386131044387TC20GENICheterozygous55720903
5131044401131044402AG20GENICheterozygous55720905
5131044403131044404AATTGT20GENICheterozygous55720907
5131056096131056097CT35GENICheterozygous55720960
5131064840131064841TC34GENICheterozygous55721015
5131066217131066218TA22GENICheterozygous55721031
5131068379131068380AC31GENICheterozygous55721053
5131075763131075764TC9GENICheterozygous55721119
5131079090131079091CT34GENICheterozygous56290590