chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124832735124832736GT14GENIChomozygous108326421
X124833115124833116GA21GENIChomozygous131249580
X124834913124834913A15GENIChomozygous131243835
X124835598124835599AG29GENIChomozygous131249581
X124837961124837962CT25GENIChomozygous131249582
X124841670124841671AT25GENIChomozygous108326427
X124844265124844266TC31GENIChomozygous108326431
X124846567124846568AG26GENIChomozygous108326433
X124847428124847429CT37GENIChomozygous108326437
X124850885124850886TG40GENICpossibly homozygous131249583
X124837316124837317CA12GENICheterozygous134473041
X124837326124837327CA13GENICheterozygous134473042
X124837749124837750A25GENIChomozygous129787274
X124856399124856400A31GENIChomozygous129787279
X124843733124843734CT23GENIChomozygous108424745
X124856660124856660CTCTCACACGTGCTTG22GENIChomozygous131243836
X124856726124856727CT21GENIChomozygous108326439
X124858341124858342AC23GENIChomozygous108326441
X124862443124862444CT22GENIChomozygous108326443
X124866433124866434CT32GENIChomozygous131249584
X124867439124867440GA30GENIChomozygous108326445
X124867794124867794TGTCCTCTTGAC35GENIChomozygous129787283
X124866105124866115TGTCTGTCTG15GENIChomozygous134470206