chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44888335148883352GA21GENICheterozygous130651159
44888335448883355CA23GENICheterozygous130651160
44888340948883410CT31GENICheterozygous128124325
44888382848883829GA48GENICheterozygous122191716
44888383048883831CT47GENICheterozygous130651161
44888438448884385GA44GENICheterozygous112639473
44888438548884386GT44GENICheterozygous112639475
44888438748884388CG44GENICheterozygous130548444
44888449248884493TA68GENICheterozygous112639485
44888451348884514AT58GENICheterozygous130303099
44888453048884531GA54GENICheterozygous113022552
44888455448884555CT43GENICheterozygous130303100
44888457848884579TA34GENICheterozygous130303101
44888458048884581CT33GENICheterozygous112639490
44888476948884770C34GENICheterozygous128031544
44888478648884787AG34GENICheterozygous128124334
44888527348885274GA27GENICheterozygous130651162
44888527748885278GC26GENICheterozygous130651163
44888529048885291TG26GENICheterozygous130651164
44888530248885303CT26GENICheterozygous130651165
44888540348885404CG31GENICheterozygous128124338
44888552748885528GA46GENICheterozygous130303103
44890983648909837TC36GENICheterozygous130303107
44891125048911251AT28GENICheterozygous130651166
44891127948911280TA24GENICheterozygous130651167
44891128048911281GT24GENICheterozygous130651168
44891327248913273GC45GENICheterozygous112639546
44891129748911298CA23GENICheterozygous130651169
44891131648911317GA21GENICheterozygous130651170
44891169148911692TA34GENICheterozygous130651171
44891186648911867AG44GENICheterozygous130651172
44891207848912079GA34GENICheterozygous128124345
44891210748912108AT32GENICheterozygous128124346
44891247848912479GA47GENICheterozygous128124348
44891374048913741GA32GENICheterozygous130548452
44891375548913756AC30GENICheterozygous130651173
44894456848944568C33GENIChomozygous128031554