chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124156901541569016TG22GENIChomozygous115330640
124157136541571366GA17GENIChomozygous115426986
124157250941572510TC20GENIChomozygous115330683
124157436541574366CG21GENIChomozygous115385488
124157483241574833GT21GENIChomozygous115330723
124157473341574734TC33GENICpossibly homozygous115704381
124157923641579237AC30GENIChomozygous115330835
124157936941579370TC21GENICheterozygous118327203
124157937341579374TC20GENICheterozygous118327204
124157970241579703TA24GENIChomozygous115330837
124158128741581288AG25GENIChomozygous115426990
124158231641582317TC40GENIChomozygous115330859
124158631441586315GA27GENIChomozygous115330869
124158640241586403AG44GENIChomozygous115385506
124158665641586657TC18GENIChomozygous115330873
124158698841586989CT24GENIChomozygous115385508
124158710441587105AG28GENIChomozygous115385510
124158716841587169CT34GENIChomozygous115385512
124158728341587284CT42GENIChomozygous115385514
124158749641587497TA31GENIChomozygous115330877
124158205941582060GA28GENIChomozygous115442004