chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123731705123731706TG30GENIChomozygous111692722
3123733271123733272T28GENICheterozygous127925833
3123733275123733276T29GENICheterozygous131627782
3123733602123733603GA50GENIChomozygous111692724
3123734009123734010AG58GENIChomozygous111692725
3123734190123734191A50GENIChomozygous127925834
3123736914123736914A58GENIChomozygous127925835
3123737968123737968G60GENIChomozygous127925836
3123738288123738289CG64GENIChomozygous111692731
3123734953123734954TC41GENIChomozygous111692726
3123734984123734985CT37GENIChomozygous111692727
3123735516123735517AG57GENIChomozygous111692728
3123735673123735674GA53GENIChomozygous111692729
3123736910123736911AG56GENIChomozygous111692730
3123738615123738616TC56GENIChomozygous111692732
3123739036123739037AT61GENIChomozygous111692733
3123739039123739040TA60GENIChomozygous111692734
3123739354123739355AG57GENIChomozygous111692735
3123739499123739500GT54GENIChomozygous111692736
3123739668123739669TC65GENIChomozygous111692737
3123740036123740037CT64GENIChomozygous111692738
3123740230123740231AG64GENIChomozygous111692739
3123740592123740593GA47GENIChomozygous111692740
3123740766123740767TC65GENIChomozygous111692741
3123741334123741335TA55GENIChomozygous111692742