chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41041676110416762CT28GENICheterozygous56746072
41041688110416882CG52GENICheterozygous56746073
41041715310417154TC34GENICheterozygous56746074
41042037910420380AG32GENICheterozygous56746084
41042590910425910AG39GENICheterozygous56746100
41042594310425944AT25GENICheterozygous56746101
41042922910429230CA18GENICheterozygous56746175
41042925310429254TC23GENICheterozygous56746176
41044508010445081GA18GENICheterozygous56746225
41044514210445143TC10GENICheterozygous56746226
41046198510461986CT16GENICheterozygous56746296
41047214210472143CT20GENICheterozygous56746347
41048533410485335CT37GENICheterozygous56746400
41048541610485417GGGAGC23GENICheterozygous60198821
41048541710485418AT20GENICheterozygous60198822
41048541910485420CT20GENICheterozygous58327092
41048542610485427CT26GENICheterozygous56746403
41048556310485564AG16GENICheterozygous56746405
41048560910485610AG28GENICheterozygous56746406
41048565510485656AC28GENICheterozygous56746407
41048586610485867CT34GENICheterozygous56746408
41048594810485949AC23GENICheterozygous56746409
41049199910492000GA15GENICheterozygous56746448