chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141041132141041133CT43GENIChomozygous115939685
7141041404141041405A26GENICheterozygous128529393
7141041587141041588AT45GENIChomozygous115939686
7141042385141042385A24GENICheterozygous132112853
7141042944141042945CA15GENICheterozygous133559347
7141043436141043437GA29GENIChomozygous115939687
7141044200141044211AAAAAGAAAAG29GENICpossibly homozygous128529394
7141044243141044244GA34GENIChomozygous115939688
7141045765141045765A46GENICpossibly homozygous128529395
7141049208141049208AGCTGGGGACCGAACCCAGGGCCTTGCGCTTGCTAGGCCAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCTCTTT1GENIChomozygous132478909
7141052572141052573C22GENIChomozygous128529396
7141053521141053522CG39GENIChomozygous115939690
7141054282141054283AG59GENIChomozygous115939691
7141056273141056274CT49GENIChomozygous115939692
7141060510141060511AG72GENIChomozygous115939693
7141061219141061219C32GENICpossibly homozygous128529397
7141062481141062484TCA40GENIChomozygous128529398
7141063700141063700TGTT44GENIChomozygous128529399
7141063969141064011TTTCCTTTTAAAAAAACGTTATCGTCAGCAAAACTAATGTTA28GENIChomozygous128529400
7141066029141066030TC59GENIChomozygous115939695
7141066780141066781CT54GENIChomozygous115939696
7141068996141068997GA54GENIChomozygous115939697
7141069363141069363TTTTTTAAATTGTCAACCGTTGTTACTGATTGGTCTCC46GENIChomozygous128529401
7141069637141069637G45GENIChomozygous128529402