chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172728737427287375AG46GENIChomozygous111012619
172729194027291941GA39GENIChomozygous111012621
172729257127292572GA61GENIChomozygous111012625
172729278927292790GA51GENIChomozygous111012628
172729281327292814AT47GENIChomozygous111012630
172729412727294128TA32GENIChomozygous111184217
172729520427295205CT42GENIChomozygous111012632
172729806627298067AG48GENIChomozygous111012634
172729953027299531AG54GENIChomozygous111012636
172730166127301662TA51GENIChomozygous111012638
172729511827295119CT40GENIChomozygous111238467
172730372727303728GA50GENIChomozygous111238469
172730374127303742GC49GENIChomozygous111238471
172729580927295810GT33GENIChomozygous111302091
172731153727311538AG46GENIChomozygous111012663
172733238927332390AG28GENICpossibly homozygous119360317
172729583627295836T32GENIChomozygous129439878
172731565827315658GAG31GENIChomozygous129439882
172731565927315659TA32GENIChomozygous129439883
172731793927317939A23GENIChomozygous129439887