chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74411163244111633TC33GENIChomozygous964216292
74411163844111639AT31GENIChomozygous964216293
74411199144111992TC24GENIChomozygous964216294
74411211644112117TG23GENIChomozygous964216295
74411319044113191GA24GENIChomozygous964216296
74411321444113215GT22GENIChomozygous964216297
74411347644113477CT22GENIChomozygous964216298
74411356144113562AC18GENICpossibly homozygous964216299
74411405344114054CG28GENIChomozygous964216300
74411413644114137GC19GENIChomozygous964216301
74411423544114236AT21GENIChomozygous964216302
74411501944115020GA22GENIChomozygous964216303
74411599044115991GT26GENIChomozygous964216304
74411648744116488GA22GENIChomozygous964216305
74411664444116645TC13GENIChomozygous964216306
74411736044117361CA23GENIChomozygous964216307
74411755044117551AT28GENIChomozygous964216308
74411763544117636TC39GENIChomozygous964216309
74411765744117658GA39GENIChomozygous964216310
74411809844118099CA27GENIChomozygous964216311
74411812144118122GA29GENIChomozygous964216312
74411855244118553CT34GENIChomozygous964216313
74411875544118756AG19GENIChomozygous964216314
74411881744118818CG16GENIChomozygous964216315
74411917244119173CT22GENIChomozygous964216316
74411917444119175GA22GENIChomozygous964216317
74411937844119379TC32GENIChomozygous964216318
74411983244119833TG13GENIChomozygous964216319
74412092244120923GC32GENIChomozygous964216320