chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
54948695349486954GA29GENIChomozygous146129698
54948747449487475CT28GENIChomozygous146129699
54948791449487915AG39GENIChomozygous146129700
54948845749488458CT24GENIChomozygous146129701
54948849849488499CT22GENIChomozygous137459471
54948902849489029AT16GENIChomozygous146129702
54948902949489030AT16GENIChomozygous137459472
54948912949489130TG19GENIChomozygous146129703
54948919849489202TCTG21GENIChomozygous146120144
54948929949489299GTGTGTGTGTGTGTGTGTGC12GENIChomozygous146120145
54948933049489331AC15GENIChomozygous146129704
54948934049489341GA15GENIChomozygous146129705
54948956549489566AG30GENIChomozygous146129706
54948985649489857GA15GENIChomozygous146129707
54949000249490003AC23GENIChomozygous146129708
54949001049490012CT23GENIChomozygous146120146
54949021449490215CT19GENIChomozygous146129709
54949052249490523CT21GENIChomozygous146129710
54949056649490567CT23GENIChomozygous146129711
54949058249490584AC25GENIChomozygous146120147
54949060049490614ACACACACACACAC24GENIChomozygous146120148
54949070149490701A25GENIChomozygous146120149
54949111349491114AG34GENIChomozygous146129712
54949122649491227GA26GENIChomozygous146129713
54949131649491317GT19GENIChomozygous146129714
54949197549491976AG26GENIChomozygous146129715
54949296349492963A12GENIChomozygous146120150
54949328249493283GA22GENIChomozygous146129716
54949384349493844AT15GENIChomozygous146129717
54949434149494342GA15GENIChomozygous146129718
54949510749495108AG17GENIChomozygous146129719
54949543849495439AG24GENIChomozygous146129720
54949580449495805AT26GENIChomozygous146129721
54949582649495827CG26GENIChomozygous137459476
54949671749496718GA19GENIChomozygous146129722
54949867949498679AGAGAC10GENIChomozygous146120151
54949869949498700AG12GENIChomozygous137459478
54949893949498940CT18GENIChomozygous146129723
54948928849489288TT7GENIChomozygous137306885
54949835349498354AG14GENIChomozygous154283831
54949835349498354A14GENICheterozygous403718536