chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118394928783949288C12GENICpossibly homozygous131109988
118394947983949479T28GENIChomozygous131109989
118394948183949481T28GENIChomozygous131109990
118395139783951398CT18GENIChomozygous115998013
118395175583951756TC25GENIChomozygous115998015
118395280983952810CT26GENIChomozygous115998017
118395306883953069AG18GENIChomozygous115998019
118395321183953212AC17GENIChomozygous115998021
118395363583953636T17GENIChomozygous131109991
118395442183954422GA11GENIChomozygous118197385
118395575983955760CT20GENIChomozygous115998023
118395584183955842GA30GENIChomozygous115998025
118395662883956629CG21GENIChomozygous115998027
118395447883954479TC11GENIChomozygous116107093
118395799783958001AAAC13GENIChomozygous131109992
118395808883958088AGGTCAGAATGTGGGGGCCTGAGCACCCCCTGGGCCCAGTACTAGCTC15GENIChomozygous131109993
118395966283959664TA19GENIChomozygous131109994
118396004383960044TA16GENIChomozygous115998031
118396100083961001GA7GENIChomozygous115998033
118396113783961138AT22GENIChomozygous115998035
118396152883961528G19GENIChomozygous131109995
118396153483961535TA20GENIChomozygous115998037
118396216083962161G15GENIChomozygous131109996
118396291683962917CT23GENIChomozygous115998039
118397207483972075AG19GENIChomozygous115998041
118397238183972382TA12GENIChomozygous115998043
118397253383972534AG16GENIChomozygous115998045
118395878883958789AC14GENIChomozygous116162563