chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108399604383996044CT55GENIChomozygous144415688
108399649883996499GA30GENIChomozygous403292527
108399649883996499G30GENICheterozygous403292528
108399650283996503GT29GENIChomozygous140904902
108399703483997035TC55GENIChomozygous144415689
108399813783998138TC67GENICpossibly homozygous144415690
108399828083998281GT47GENICpossibly homozygous144415691
108399843483998435CG50GENIChomozygous144415692
108399892583998926GA52GENIChomozygous144415693
108399739883997399TG56GENICpossibly homozygous138836623
108399843383998434A49GENIChomozygous144412169
108399997983999979AAAAG6GENICheterozygous144412170
108400048984000490AG34GENIChomozygous138836628
108400053184000532A25GENICpossibly homozygous138695375
108400055484000554C32GENIChomozygous144412171
108400057284000573C35GENIChomozygous138695376
108400089884000899CG63GENIChomozygous144415694
108400119884001198TG60GENIChomozygous144412172
108400207084002070A61GENIChomozygous144412174
108400287484002875AG53GENIChomozygous144415695
108400318684003187GC55GENIChomozygous144415696
108400352684003527CT55GENIChomozygous144415697
108400378084003781C34GENICpossibly homozygous403292531
108400378084003781CG34GENICheterozygous403292532
108400382984003830CA40GENIChomozygous144415698
108400403984004040AG49GENIChomozygous138836632
108400404184004042TC49GENIChomozygous144415699
108400445484004455TC53GENICpossibly homozygous144415700
108400450984004510CA54GENICpossibly homozygous144415701
108400454484004545TC55GENIChomozygous144415702
108400466784004668AT44GENIChomozygous144415703
108400479584004799TATT52GENIChomozygous144412175
108400495684004957CT56GENIChomozygous144415704
108400501884005019CT43GENIChomozygous144415705
108400589584005896TG49GENIChomozygous138836634
108400716884007169TA45GENIChomozygous138836636
108400479884004799T52GENIChomozygous403938623
108400479884004799TC52GENICheterozygous403938624