chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4256026042560261AG7GENIChomozygous108486720
X4256027742560277A6GENIChomozygous132778476
X4256152042561520C3GENICheterozygous130719497
X4256344542563446T10GENIChomozygous133454043
X4256881042568821GATCTGTTTAC10GENIChomozygous133454044
X4256961542569616AG6GENIChomozygous108731825
X4256970442569704GAGAGAGAGAG6GENICheterozygous133695310
X4257376342573763TG9GENIChomozygous133454045
X4257483842574839AG10GENIChomozygous108486758
X4257838242578383CT10GENIChomozygous108486768
X4258245442582455CT11GENIChomozygous108486774
X4258662142586622AG8GENIChomozygous108486778
X4256489242564893TG9GENIChomozygous108705962
X4258289142582892AG9GENIChomozygous108705964
X4256942142569422TA1GENIChomozygous133458911
X4256942342569424TA1GENIChomozygous133458912
X4256942542569426TA1GENIChomozygous133458913
X4258725542587255T10GENIChomozygous133454046
X4258819242588193CT13GENIChomozygous108705966
X4258905242589057GTGTA11GENIChomozygous133454047
X4259053342590534TC12GENIChomozygous108705968
X4259249542592496A1GENIChomozygous129738793
X4259249942592500A1GENIChomozygous129738794
X4259250542592505G1GENIChomozygous129738795
X4259251842592518TTT2GENIChomozygous129738796
X4259306642593067AG8GENIChomozygous108672155
X4259707442597075GA6GENIChomozygous108486786
X4259721042597211CG5GENIChomozygous108672158
X4259817642598177CA10GENIChomozygous108705970
X4259887242598873CG2GENIChomozygous108256997
X4259998142599982AC5GENIChomozygous108731827
X4260575642605757CA13GENIChomozygous108486788