chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145472369145472370TC22GENIChomozygous112870906
4145472965145472966CA19GENIChomozygous113179000
4145473165145473166TA18GENIChomozygous113179001
4145476776145476777GT22GENIChomozygous113179002
4145477153145477154TC18GENIChomozygous113179003
4145477809145477810GA19GENIChomozygous113179004
4145477850145477851AG24GENIChomozygous113179005
4145479385145479386CT19GENIChomozygous113179006
4145480529145480530TC25GENIChomozygous112870909
4145481733145481734CT23GENIChomozygous112870910
4145481748145481749CG21GENIChomozygous112870911
4145485656145485657CT20GENIChomozygous112870914
4145485793145485794GT28GENIChomozygous112870915
4145485847145485848AT29GENIChomozygous113179007
4145486325145486326GT16GENIChomozygous112870917
4145486784145486785GC22GENIChomozygous112870918
4145486793145486794GC22GENIChomozygous112870919