chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84450310144503102CT16GENIChomozygous641618607
84450321244503213TTA16GENIChomozygous752014564
84450324744503248TC13GENIChomozygous641618608
84450432844504329GGA18GENIChomozygous752014566
84450467444504675TC14GENIChomozygous641618609
84450530544505306AG18GENIChomozygous641618610
84450660744506608CT20GENIChomozygous641618611
84450710644507107TC25GENIChomozygous641618612
84450792544507926TC15GENIChomozygous641618613
84450956044509561GA17GENIChomozygous641618614
84450957244509573GT18GENIChomozygous641618615
84450992644509927GC20GENIChomozygous641618616
84451006244510063GA15GENIChomozygous641618617
84451020744510208TC15GENIChomozygous641618618
84451076344510764GA17GENIChomozygous641618619
84451173744511738AG30GENIChomozygous641618620
84451224744512248TTACACAC4GENICheterozygous752014570
84451292044512921AT14GENIChomozygous641618621
84451312444513128TTTA----14GENICpossibly homozygous752014571
84451328644513287AC8GENIChomozygous641618622
84451363044513631TA21GENIChomozygous641618623
84451376644513767CCA21GENICpossibly homozygous752014572
84451504244515043TC16GENIChomozygous641618624
84451512844515129GA14GENIChomozygous641618625
84451534044515344TTTA----10GENICheterozygous752014574
84451572844515729CCTGCTTGCTAGGCAAG5GENIChomozygous752014576
84451653744516538AT16GENIChomozygous641618626