chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124832735124832736GT26GENIChomozygous108326421
X124837749124837750A23GENIChomozygous129787274
X124837950124837950ATAC13GENIChomozygous129787275
X124841051124841051TTAAATA13GENIChomozygous129787276
X124841670124841671AT18GENIChomozygous108326427
X124841779124841780CG26GENIChomozygous108326429
X124844265124844266TC26GENIChomozygous108326431
X124846567124846568AG26GENIChomozygous108326433
X124847011124847012GA26GENIChomozygous108326435
X124847428124847429CT18GENIChomozygous108326437
X124850004124850005A30GENICpossibly homozygous129787277
X124853953124853958AAAAC26GENIChomozygous129787278
X124856399124856400A25GENIChomozygous129787279
X124856655124856655GT18GENIChomozygous129787280
X124856726124856727CT20GENIChomozygous108326439
X124858341124858342AC24GENIChomozygous108326441
X124862366124862366A15GENIChomozygous129787281
X124862443124862444CT33GENIChomozygous108326443
X124865594124865594A9GENICpossibly homozygous129787282
X124867439124867440GA24GENIChomozygous108326445
X124867794124867794TGTCCTCTTGAC22GENIChomozygous129787283
X124843733124843734CT31GENIChomozygous108424745
X124850360124850360A21GENICheterozygous130804313