chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104018668840186689CA18GENIChomozygous116568737
104018701440187015CT19GENIChomozygous116568739
104018754340187544CT17GENIChomozygous116927430
104018791540187916CT20GENIChomozygous118065926
104018797740187978CT17GENIChomozygous116927432
104019017840190179TG18GENICpossibly homozygous116927434
104019088340190884GA18GENIChomozygous117141355
104019212040192121TA25GENIChomozygous116927436
104019227940192280AC11GENIChomozygous116977336
104019271240192712A14GENIChomozygous131901725
104019350940193510AT13GENIChomozygous116927438
104019352640193527GA16GENIChomozygous116927440
104019424740194248AG16GENIChomozygous116927442
104019453340194534TC12GENIChomozygous116763930
104019458040194581AG21GENIChomozygous116568745
104019472440194725AG23GENIChomozygous116927444
104019475240194753TA22GENIChomozygous116927446
104019475840194759AT22GENIChomozygous116977338
104019540940195524AACACTTAAGATTCTTTTTTTTTTTTTGGTTCTTTTTTTTCGGAACTAGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCAAGCCCC15GENIChomozygous131091682
104019592340195924TC17GENIChomozygous116763934
104019647640196477TA22GENIChomozygous116927448
104019769240197699AAAAAAG10GENICheterozygous132881357
104019827740198278AG17GENIChomozygous116927450
104019837640198376AAC11GENIChomozygous131901726
104019991240199913CT26GENIChomozygous116927452
104020044340200444A18GENIChomozygous132691043
104020134240201343AG17GENIChomozygous116927454
104020058340200584AG22GENIChomozygous117057559
104019211340192114AT27GENIChomozygous116870414
104019249440192494A11GENICpossibly homozygous128809811
104020058040200581CT24GENIChomozygous117057555
104020058140200582AG23GENIChomozygous117057557