chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139371696393716964GA21GENICheterozygous49965839
139371784993717850AAG24GENICheterozygous49965840
139371812493718125GA12GENICheterozygous50982768
139371851493718515TC18GENICheterozygous50838220
139371860093718601TC16GENICheterozygous49965841
139371897093718971CT17GENICheterozygous49965842
139371908993719090TC18GENICheterozygous50982770
139371922493719225TC12GENICheterozygous50982771
139371953893719539GA12GENICheterozygous49965844
139371999193719992TC9GENICheterozygous49965846
139372302893723029TC16GENICheterozygous50982772
139372318093723181CG19GENICheterozygous50982773
139372337993723380AC10GENICheterozygous49965848
139372367093723671TG17GENICheterozygous50982774
139372387293723873GC11GENICheterozygous49965852
139372616593726166GT10GENICheterozygous49859910
139373011093730111AT11GENICheterozygous49965867
139373011193730112AT12GENICheterozygous50982775
139373059793730598TG18GENICheterozygous50982776
139373065293730653TC21GENICheterozygous49965868
139373098993730990GC18GENICheterozygous49965869
139373120293731203CCA20GENICheterozygous50982777
139373432593734326CA25GENICheterozygous50982778
139373439393734394CT25GENICheterozygous49965872
139373465993734660TC17GENICheterozygous49965873
139373572493735725TTCTGG18GENICheterozygous49965875
139373639493736395CT11GENICheterozygous51281733
139373640493736405CG11GENICheterozygous51281734
139373640693736407CG17GENICheterozygous51281735
139373641293736413AG17GENICheterozygous50497466