chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6125042349125042350AT26GENIChomozygous955280240
6125043149125043150GT35GENIChomozygous955280241
6125045107125045108CT31GENIChomozygous955280242
6125048772125048773GA20GENIChomozygous955280243
6125049812125049813TC25GENIChomozygous955280244
6125051702125051703TC34GENICpossibly homozygous955280245
6125051787125051788GA23GENIChomozygous955280246
6125052367125052368TC20GENIChomozygous955280247
6125052674125052675CT19GENIChomozygous955280248
6125052929125052930CT11GENIChomozygous955280249
6125053620125053621AG17GENIChomozygous955280250
6125054104125054105CT20GENIChomozygous955280251
6125058255125058256GA11GENIChomozygous955280252
6125061110125061111GT16GENIChomozygous955280253
6125064989125064990GA22GENIChomozygous955280254
6125066295125066296TC20GENIChomozygous955280255
6125067010125067011AC26GENIChomozygous955280256
6125067989125067990CT23GENIChomozygous955280257
6125068238125068239CT21GENIChomozygous955280258
6125068645125068646CT22GENIChomozygous955280259
6125069020125069021TC11GENIChomozygous955280260
6125069192125069193CG15GENIChomozygous955280261
6125070462125070463GA28GENIChomozygous955280262
6125070954125070955CT26GENIChomozygous955280263
6125072010125072011GC22GENIChomozygous955280264
6125073846125073847CT27GENIChomozygous955280265
6125075490125075491GA39GENIChomozygous955280266
6125077163125077164TA17GENIChomozygous955280267
6125078090125078091AG26GENIChomozygous955280268
6125081226125081227AC19GENIChomozygous955280269