chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123731705123731706TG16GENIChomozygous111692722
3123733271123733272T7GENICheterozygous127925833
3123733602123733603GA31GENIChomozygous111692724
3123734009123734010AG37GENIChomozygous111692725
3123734190123734191A17GENIChomozygous127925834
3123734953123734954TC19GENIChomozygous111692726
3123734984123734985CT18GENIChomozygous111692727
3123735516123735517AG19GENIChomozygous111692728
3123735673123735674GA14GENIChomozygous111692729
3123736910123736911AG22GENIChomozygous111692730
3123736914123736914A22GENIChomozygous127925835
3123737930123737931CT26GENIChomozygous119702626
3123737968123737968G25GENIChomozygous127925836
3123738288123738289CG31GENIChomozygous111692731
3123738615123738616TC27GENIChomozygous111692732
3123739036123739037AT24GENIChomozygous111692733
3123739039123739040TA24GENIChomozygous111692734
3123739354123739355AG19GENIChomozygous111692735
3123739499123739500GT18GENIChomozygous111692736
3123739668123739669TC24GENIChomozygous111692737
3123740036123740037CT14GENIChomozygous111692738
3123741334123741335TA30GENIChomozygous111692742
3123740230123740231AG21GENIChomozygous111692739
3123740592123740593GA29GENIChomozygous111692740
3123740766123740767TC22GENIChomozygous111692741