chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69180265591802656T24GENICpossibly homozygous137696947
69180302991803030TC23GENIChomozygous141847466
69180348691803487GT26GENIChomozygous141847467
69180717891807179AG26GENIChomozygous141847468
69180737391807374CT20GENIChomozygous141847469
69180865191808652T25GENICpossibly homozygous137696949
69180946391809464T21GENIChomozygous137696950
69181018991810190AC5GENICheterozygous141847470
69181426091814261CG20GENICpossibly homozygous141847471
69181450591814506CT28GENIChomozygous141847472
69181426391814275CCCAAGCAGCGA20GENICpossibly homozygous141784070