chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152629154152629155TTTCTC19GENICheterozygous55798916
5152629155152629157TC--19GENICpossibly homozygous55798917
5152629199152629201TT--35GENICheterozygous55798918
5152631232152631233CCCTT23GENIChomozygous55798919
5152631235152631238CCT---22GENIChomozygous55798920
5152634033152634034CCA21GENIChomozygous55798921
5152634877152634878TG32GENICheterozygous55798922
5152648091152648093TG--15GENICpossibly homozygous55798923
5152648907152648908AG24GENIChomozygous55798924
5152648909152648910G-23GENIChomozygous55798925
5152648918152648919GA23GENIChomozygous55798926
5152648927152648928CT15GENIChomozygous55798927
5152648929152648930CT16GENIChomozygous55798928
5152649831152649835TGTG----5GENICheterozygous55798929
5152649833152649835TG--5GENICheterozygous55798930
5152651405152651406TTG4GENICheterozygous55798931
5152657114152657115TC61GENIChomozygous55798932
5152658002152658003AG48GENIChomozygous55798933