chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129795360129795361TC12GENIChomozygous604227403
7129795406129795407A-26GENICpossibly homozygous729229205
7129795959129795960TTTGGG7GENIChomozygous729229206
7129795961129795962AATTTAGCTCAGTGGTAGAGCGCTTGCCTAG7GENIChomozygous729229207
7129796093129796094AT16GENIChomozygous604227404
7129796801129796803CC--9GENICheterozygous729229208
7129796802129796803C-9GENICheterozygous729229209
7129797073129797074GA18GENIChomozygous604227405
7129798576129798577AAAAGC10GENIChomozygous729229212
7129798798129798802GAAG----6GENICheterozygous729229214
7129800366129800367T-14GENIChomozygous729229216
7129800826129800827CCAT4GENIChomozygous729229218
7129801567129801568G-5GENIChomozygous729229220
7129802532129802533TC22GENIChomozygous604227406
7129803707129803708TA30GENIChomozygous604227407
7129803754129803755AC37GENIChomozygous604227408
7129804462129804465CAC---14GENICpossibly homozygous729229221