chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6125042349125042350AT21GENIChomozygous958252287
6125043149125043150GT30GENIChomozygous958252288
6125045107125045108CT23GENIChomozygous958252289
6125048772125048773GA28GENIChomozygous958252290
6125049812125049813TC28GENIChomozygous958252291
6125051702125051703TC32GENIChomozygous958252292
6125051787125051788GA29GENIChomozygous958252293
6125052674125052675CT12GENIChomozygous958252294
6125052929125052930CT16GENIChomozygous958252295
6125053620125053621AG27GENIChomozygous958252296
6125054104125054105CT20GENIChomozygous958252297
6125058255125058256GA21GENIChomozygous958252298
6125061110125061111GT19GENIChomozygous958252299
6125064989125064990GA16GENIChomozygous958252300
6125066295125066296TC21GENIChomozygous958252301
6125067010125067011AC29GENIChomozygous958252302
6125067989125067990CT19GENIChomozygous958252303
6125068238125068239CT12GENIChomozygous958252304
6125068645125068646CT29GENIChomozygous958252305
6125069020125069021TC14GENIChomozygous958252306
6125069192125069193CG20GENIChomozygous958252307
6125070462125070463GA29GENIChomozygous958252308
6125070954125070955CT21GENIChomozygous958252309
6125072010125072011GC26GENIChomozygous958252310
6125073846125073847CT32GENIChomozygous958252311
6125075490125075491GA43GENIChomozygous958252312
6125077163125077164TA20GENIChomozygous958252313
6125078090125078091AG17GENIChomozygous958252314
6125081226125081227AC19GENIChomozygous958252315