chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X155850857155850858AC4GENIChomozygous108353948
X155852254155852255GT4GENICheterozygous108353965
X155853722155853723GA14GENICpossibly homozygous108600118
X155853834155853835AC6GENICheterozygous108353983
X155853866155853867CG10GENICheterozygous108353985
X155853893155853894TG11GENICheterozygous108353987
X155854003155854004AT13GENICheterozygous108600120
X155854464155854465AG7GENICheterozygous108353995
X155854856155854857CT20GENICheterozygous108600122
X155855115155855116TC14GENICheterozygous108600124
X155856180155856181TC6GENICheterozygous108600128
X155856212155856213GA8GENICheterozygous108600130
X155856276155856277AG7GENICheterozygous108354007
X155857690155857691AC7GENICheterozygous108600132
X155857691155857692GC7GENICheterozygous108600134
X155857906155857907CT5GENICheterozygous108600136
X155860320155860321CT3GENIChomozygous108429380
X155860896155860897CG5GENIChomozygous108354029
X155860897155860898GA5GENIChomozygous108354031