chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141041132141041133CT14GENIChomozygous115939685
7141041404141041405A9GENIChomozygous128529393
7141041587141041588AT17GENIChomozygous115939686
7141043436141043437GA10GENIChomozygous115939687
7141044200141044211AAAAAGAAAAG12GENICheterozygous128529394
7141044243141044244GA14GENIChomozygous115939688
7141045765141045765A8GENIChomozygous128529395
7141052572141052573C7GENIChomozygous128529396
7141053521141053522CG21GENIChomozygous115939690
7141054282141054283AG19GENIChomozygous115939691
7141056273141056274CT19GENIChomozygous115939692
7141060510141060511AG13GENIChomozygous115939693
7141061219141061219C8GENICpossibly homozygous128529397
7141062481141062484TCA14GENIChomozygous128529398
7141063700141063700TGTT18GENIChomozygous128529399
7141063969141064011TTTCCTTTTAAAAAAACGTTATCGTCAGCAAAACTAATGTTA9GENIChomozygous128529400
7141066029141066030TC9GENIChomozygous115939695
7141066780141066781CT25GENIChomozygous115939696
7141068996141068997GA20GENIChomozygous115939697
7141069363141069363TTTTTTAAATTGTCAACCGTTGTTACTGATTGGTCTCC14GENIChomozygous128529401
7141069637141069637G25GENIChomozygous128529402