chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123731705123731706TG11GENIChomozygous111692722
3123733271123733272T11GENIChomozygous127925833
3123733602123733603GA19GENIChomozygous111692724
3123734009123734010AG13GENIChomozygous111692725
3123734190123734191A15GENIChomozygous127925834
3123734953123734954TC13GENIChomozygous111692726
3123734984123734985CT13GENIChomozygous111692727
3123735516123735517AG18GENIChomozygous111692728
3123735673123735674GA14GENIChomozygous111692729
3123736910123736911AG23GENIChomozygous111692730
3123736914123736914A24GENIChomozygous127925835
3123737968123737968G15GENIChomozygous127925836
3123738288123738289CG27GENIChomozygous111692731
3123738615123738616TC21GENIChomozygous111692732
3123739036123739037AT28GENIChomozygous111692733
3123739039123739040TA28GENIChomozygous111692734
3123739354123739355AG20GENIChomozygous111692735
3123739499123739500GT19GENIChomozygous111692736
3123739668123739669TC18GENIChomozygous111692737
3123740036123740037CT15GENIChomozygous111692738
3123740230123740231AG15GENIChomozygous111692739
3123740592123740593GA14GENIChomozygous111692740
3123740766123740767TC15GENIChomozygous111692741
3123741334123741335TA11GENIChomozygous111692742
3123737930123737931CT17GENIChomozygous119702626