chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124688168746881688TC26GENIChomozygous115486536
124688345246883453GC28GENIChomozygous115342657
124688365146883652TC35GENIChomozygous115397205
124688519746885198CA29GENIChomozygous133011101
124688519846885199AG30GENIChomozygous133011102
124688371546883716GT17GENIChomozygous118272517
124688375446883755TC14GENIChomozygous118272518
124688522946885230GA37GENIChomozygous118272521
124688417146884177GAGAGC6GENIChomozygous133912353
124688523846885239TC36GENIChomozygous133011103
124688574546885746AG38GENIChomozygous115397207
124688574946885750AC38GENIChomozygous115397209
124688575446885755G38GENIChomozygous133010135
124688574046885740CT37GENIChomozygous133010132
124688574846885748ACAC38GENIChomozygous133010133
124688575246885752TGCGATCT38GENIChomozygous133010134
124688662846886629GT37GENIChomozygous115486537
124688683146886832T35GENIChomozygous128996762
124688860346888711AGTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCG25GENIChomozygous128996764
124688900346889004GT36GENIChomozygous115486539
124688929246889293TC36GENIChomozygous115342671
124688967746889678GA44GENIChomozygous115342673
124688960246889603AG41GENIChomozygous115480594