chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152629155152629157TC--3GENIChomozygous55798917
5152631232152631235CTC---29GENIChomozygous56461209
5152631237152631238TTTTC34GENIChomozygous56461210
5152634033152634034CCA4GENIChomozygous55798921
5152648091152648095TGTG----15GENICheterozygous56495059
5152648093152648095TG--15GENICpossibly homozygous56495060
5152648907152648908AG29GENIChomozygous55798924
5152648909152648910G-30GENIChomozygous55798925
5152648911152648912CT30GENIChomozygous56356601
5152648916152648917CCTAAAT29GENIChomozygous56356602
5152648920152648925AGGCC-----29GENIChomozygous56356604
5152648927152648928CT28GENIChomozygous55798927
5152648929152648930CT27GENIChomozygous55798928
5152649837152649845TGTGTGTG--------4GENICheterozygous56461217
5152649843152649845TG--4GENICheterozygous56495061
5152651405152651406TTG2GENIChomozygous55798931
5152652842152652843T-14GENICheterozygous56532786
5152657114152657115TC38GENIChomozygous55798932
5152658002152658003AG24GENIChomozygous55798933