chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6125042349125042350AT13GENIChomozygous789939248
6125043149125043150GT28GENIChomozygous789939249
6125045107125045108CT33GENIChomozygous789939250
6125048772125048773GA14GENIChomozygous789939251
6125049812125049813TC18GENIChomozygous789939252
6125051702125051703TC23GENIChomozygous789939253
6125051787125051788GA24GENIChomozygous789939254
6125052367125052368TC21GENIChomozygous789939255
6125052674125052675CT14GENIChomozygous789939256
6125052929125052930CT21GENIChomozygous789939257
6125053620125053621AG21GENIChomozygous789939258
6125054104125054105CT17GENIChomozygous789939259
6125058255125058256GA16GENIChomozygous789939260
6125061110125061111GT11GENIChomozygous789939261
6125064989125064990GA17GENIChomozygous789939262
6125066295125066296TC9GENIChomozygous789939263
6125067010125067011AC24GENIChomozygous789939264
6125067226125067227GA29GENICheterozygous789939265
6125067234125067235AG25GENICheterozygous789939266
6125067238125067239AG28GENICheterozygous789939267
6125067989125067990CT18GENIChomozygous789939268
6125068238125068239CT16GENIChomozygous789939269
6125069020125069021TC13GENIChomozygous789939270
6125069192125069193CG21GENIChomozygous789939271
6125070462125070463GA29GENIChomozygous789939272
6125070954125070955CT21GENIChomozygous789939273
6125072010125072011GC14GENIChomozygous789939274
6125073846125073847CT30GENIChomozygous789939275
6125075490125075491GA34GENIChomozygous789939276
6125077163125077164TA10GENIChomozygous789939277
6125077737125077738GA20GENIChomozygous789939278
6125078090125078091AG22GENIChomozygous789939279
6125081226125081227AC23GENIChomozygous789939280