chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141874744141874745G50GENIChomozygous127439479
1141875874141875875TC56GENIChomozygous108262001
1141877608141877609AG50GENIChomozygous108262015
1141880006141880007CT55GENIChomozygous108262017
1141882243141882244AT38GENIChomozygous108262041
1141882348141882348G27GENIChomozygous127439486
1141876295141876296CA51GENICpossibly homozygous109327770
1141876467141876468GA45GENIChomozygous109327771
1141877015141877015CG24GENICpossibly homozygous130823656
1141882312141882312G24GENIChomozygous127439485
1141882352141882353GT32GENIChomozygous121086506
1141882354141882355A33GENIChomozygous127439487
1141882377141882377T33GENIChomozygous127439488
1141882390141882391TC31GENIChomozygous108262045
1141884698141884699CT46GENIChomozygous109327773
1141885436141885437TA48GENIChomozygous108262069
1141887085141887086GA36GENIChomozygous109327774
1141887521141887522A35GENIChomozygous130823657
1141890423141890424AG49GENIChomozygous108262093