chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145471891145471892CT9GENIChomozygous119315545
4145472230145472231CT8GENIChomozygous119315546
4145472369145472370TC7GENIChomozygous112870906
4145476776145476777GT20GENIChomozygous113179002
4145477153145477154TC8GENIChomozygous113179003
4145477850145477851AG9GENIChomozygous113179005
4145480158145480159GA12GENIChomozygous119315547
4145480529145480530TC10GENIChomozygous112870909
4145481623145481624AG20GENIChomozygous119315548
4145481733145481734CT10GENIChomozygous112870910
4145481748145481749CG7GENIChomozygous112870911
4145482380145482381TA7GENIChomozygous119315549
4145482848145482849CT12GENIChomozygous119315550
4145485492145485493TC7GENIChomozygous119315551
4145485656145485657CT11GENIChomozygous112870914
4145485793145485794GT11GENIChomozygous112870915
4145486088145486089CG11GENIChomozygous113179008
4145486325145486326GT11GENIChomozygous112870917
4145486784145486785GC13GENIChomozygous112870918