chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141041132141041133CT18GENIChomozygous115939685
7141041404141041405A8GENIChomozygous128529393
7141041587141041588AT8GENIChomozygous115939686
7141042471141042472AG13GENICheterozygous130359631
7141042475141042476CT14GENICheterozygous130359632
7141043436141043437GA12GENIChomozygous115939687
7141044200141044211AAAAAGAAAAG5GENIChomozygous128529394
7141044243141044244GA9GENIChomozygous115939688
7141045765141045765A15GENIChomozygous128529395
7141052572141052573C13GENIChomozygous128529396
7141053521141053522CG11GENIChomozygous115939690
7141054282141054283AG15GENIChomozygous115939691
7141056273141056274CT17GENIChomozygous115939692
7141060510141060511AG13GENIChomozygous115939693
7141061219141061219C11GENIChomozygous128529397
7141062481141062484TCA15GENIChomozygous128529398
7141063700141063700TGTT13GENIChomozygous128529399
7141063969141064011TTTCCTTTTAAAAAAACGTTATCGTCAGCAAAACTAATGTTA11GENIChomozygous128529400
7141066029141066030TC21GENIChomozygous115939695
7141066780141066781CT14GENIChomozygous115939696
7141068996141068997GA13GENIChomozygous115939697
7141069363141069363TTTTTTAAATTGTCAACCGTTGTTACTGATTGGTCTCC19GENIChomozygous128529401
7141069637141069637G11GENIChomozygous128529402