chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6125042349125042350AT73GENIChomozygous780590325
6125043149125043150GT51GENIChomozygous780590326
6125045107125045108CT65GENICpossibly homozygous780590327
6125048772125048773GA38GENIChomozygous780590328
6125049812125049813TC80GENIChomozygous780590329
6125051702125051703TC80GENIChomozygous780590330
6125051787125051788GA80GENIChomozygous780590331
6125052367125052368TC59GENIChomozygous780590332
6125052674125052675CT51GENIChomozygous780590333
6125052929125052930CT49GENIChomozygous780590334
6125053620125053621AG61GENIChomozygous780590335
6125054104125054105CT79GENIChomozygous780590336
6125057952125057953GC10GENICheterozygous780590337
6125058255125058256GA68GENIChomozygous780590338
6125061110125061111GT59GENIChomozygous780590339
6125064989125064990GA54GENICpossibly homozygous780590340
6125066295125066296TC64GENICpossibly homozygous780590341
6125067010125067011AC65GENIChomozygous780590342
6125067226125067227GA22GENICheterozygous780590343
6125067234125067235AG20GENICheterozygous780590344
6125067238125067239AG20GENICheterozygous780590345
6125067989125067990CT73GENIChomozygous780590346
6125068238125068239CT67GENICpossibly homozygous780590347
6125069020125069021TC63GENIChomozygous780590348
6125069192125069193CG97GENIChomozygous780590349
6125070462125070463GA81GENIChomozygous780590350
6125070954125070955CT80GENIChomozygous780590351
6125072010125072011GC54GENIChomozygous780590352
6125073846125073847CT36GENIChomozygous780590353
6125075490125075491GA43GENIChomozygous780590354
6125077163125077164TA50GENIChomozygous780590355
6125077737125077738GA33GENICpossibly homozygous780590356
6125078090125078091AG66GENIChomozygous780590357
6125081226125081227AC90GENIChomozygous780590358