chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145472369145472370TC64GENIChomozygous112870906
4145472937145472938A42GENIChomozygous128087995
4145477153145477154TC43GENIChomozygous113179003
4145472965145472966CA49GENIChomozygous113179000
4145473165145473166TA46GENIChomozygous113179001
4145476776145476777GT58GENIChomozygous113179002
4145473627145473627A45GENIChomozygous130938720
4145476316145476316G12GENIChomozygous130938721
4145476319145476319GGG12GENIChomozygous130938722
4145477809145477810GA44GENICpossibly homozygous113179004
4145477850145477851AG51GENIChomozygous113179005
4145479385145479386CT37GENIChomozygous113179006
4145480529145480530TC54GENIChomozygous112870909
4145481733145481734CT50GENICpossibly homozygous112870910
4145481748145481749CG47GENIChomozygous112870911
4145482481145482484AAC39GENIChomozygous130938723
4145483295145483295AT45GENICheterozygous132606899
4145485656145485657CT43GENIChomozygous112870914
4145485793145485794GT56GENIChomozygous112870915
4145485847145485848AT50GENIChomozygous113179007
4145486088145486089CG45GENIChomozygous113179008
4145486325145486326GT60GENIChomozygous112870917
4145486784145486785GC43GENIChomozygous112870918
4145486793145486794GC47GENIChomozygous112870919