chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X128897596128897597TC13GENIChomozygous108332625
X128898443128898444CT9GENIChomozygous108332627
X128898578128898579TC13GENIChomozygous108332629
X128901952128901953AG16GENIChomozygous108332631
X128907309128907310AT18GENIChomozygous108332633
X128907735128907735T14GENIChomozygous129789511
X128898905128898905GATT11GENIChomozygous129789508
X128901659128901659CTC5GENIChomozygous129789509
X128901683128901683T3GENIChomozygous129789510
X128909377128909378TC17GENIChomozygous108332635
X128909769128909770T7GENIChomozygous130195768
X128910718128910719TA12GENIChomozygous108332637
X128911867128911868TC13GENIChomozygous108332639
X128912122128912123C12GENIChomozygous129789512
X128913352128913352T12GENICheterozygous129789513
X128914133128914134TC12GENIChomozygous108332641
X128916365128916366CT9GENIChomozygous108332643
X128909772128909773TC7GENIChomozygous108425753
X128909802128909803AC2GENIChomozygous130203017
X128921502128921502A6GENIChomozygous129789514
X128924540128924541T9GENIChomozygous129789515