chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145472369145472370TC20GENIChomozygous112870906
4145472937145472938A29GENIChomozygous128087995
4145472965145472966CA37GENIChomozygous113179000
4145473165145473166TA23GENIChomozygous113179001
4145476776145476777GT20GENIChomozygous113179002
4145477153145477154TC35GENIChomozygous113179003
4145477809145477810GA28GENIChomozygous113179004
4145477850145477851AG30GENIChomozygous113179005
4145479385145479386CT22GENIChomozygous113179006
4145480529145480530TC21GENICpossibly homozygous112870909
4145481733145481734CT29GENIChomozygous112870910
4145481748145481749CG26GENIChomozygous112870911
4145483295145483295AT22GENICheterozygous132606899
4145485656145485657CT24GENIChomozygous112870914
4145485793145485794GT37GENIChomozygous112870915
4145485847145485848AT35GENIChomozygous113179007
4145486088145486089CG28GENIChomozygous113179008
4145486325145486326GT31GENIChomozygous112870917
4145486784145486785GC21GENIChomozygous112870918
4145486793145486794GC20GENIChomozygous112870919
4145473627145473627A33GENIChomozygous130938720
4145476316145476316G17GENIChomozygous130938721
4145476319145476319GGG17GENIChomozygous130938722
4145482481145482484AAC15GENIChomozygous130938723