chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75498645054986451TTTG9INTERGENICpossibly homozygous54736011
75499152754991528AAT5INTERGENIChomozygous54976700
75499152954991530AATTTATTCTCTAACTAGACATGGACATCGGAATAAAAAATGGTGGGTTTGAATAATATCAGTTTTTCT5INTERGENIChomozygous54976702
75499388354993891CTATCTAT--------6INTERGENICheterozygous55024590
75499388754993891CTAT----6INTERGENICheterozygous54976704
75500445955004537TTTAGTTTCACTTTTTTCTCCATCTTATTAAATTGAGTATCTCTTATTTACATTTCAATTGTTATTCCCTTTCCCCAG------------------------------------------------------------------------------13GENIChomozygous54902821
75501969755019699GT--9GENICheterozygous54976710
75502466955024670GGCTTGCTA7GENIChomozygous53929092
75502467155024672GGCAAGCGCTCTACCACTGAGCTAAATCCCC6GENIChomozygous54976712
75502504955025051AC--13GENICheterozygous54976714
75502962355029629TATATC------2GENIChomozygous55024592
75503340755033409CA--21GENICheterozygous54976716
75504093155040932GGT3GENICheterozygous54976718
75504738655047387CCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT1GENIChomozygous54976722
75505317055053171C-24GENIChomozygous54976724
75505317555053176CCT25GENIChomozygous54976726
75506830555068306CCGCACCCTTTGCTTTCTCTTTCCCAAGATTCAGCCAATTGGAGGAGCGGACAGGGATCAGAACCCACCCCCAGGCATCT15GENIChomozygous54976729
75507391155073912GGTCTA13GENICheterozygous54976731
75509650555096507AA--2GENIChomozygous53929101
75511818755118188AATT11GENICheterozygous55141685
75511819055118191T-11GENICheterozygous55141686
75512775355127755TC--14GENICheterozygous54976735
75512969555129696CCATTT4GENICheterozygous55622716
75515260055152601C-18GENIChomozygous53929123