chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75499152754991528AAT7INTERGENIChomozygous54976700
75499152954991530AATTTATTCTCTAACTAGACATGGACATCGGAATAAAAAATGGTGGGTTTGAATAATATCAGTTTTTCT7INTERGENIChomozygous54976702
75499388754993891CTAT----2INTERGENIChomozygous54976704
75499651754996518GGCA10INTERGENICheterozygous54976706
75499651854996520CA--10INTERGENICheterozygous54976708
75500445955004537TTTAGTTTCACTTTTTTCTCCATCTTATTAAATTGAGTATCTCTTATTTACATTTCAATTGTTATTCCCTTTCCCCAG------------------------------------------------------------------------------9GENIChomozygous54902821
75501969755019699GT--14GENICheterozygous54976710
75502466955024670GGCTTGCTA6GENIChomozygous53929092
75502467155024672GGCAAGCGCTCTACCACTGAGCTAAATCCCC6GENIChomozygous54976712
75502504955025051AC--6GENICheterozygous54976714
75503340755033409CA--10GENICheterozygous54976716
75503958855039589CCT7GENICheterozygous54195895
75504093155040932GGT1GENIChomozygous54976718
75504445555044456TTACACAC3GENICheterozygous54976720
75504738655047387CCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT6GENIChomozygous54976722
75505317055053171C-13GENIChomozygous54976724
75505317555053176CCT16GENIChomozygous54976726
75506830555068306CCGCACCCTTTGCTTTCTCTTTCCCAAGATTCAGCCAATTGGAGGAGCGGACAGGGATCAGAACCCACCCCCAGGCATCT12GENIChomozygous54976729
75507391155073912GGTCTA12GENICpossibly homozygous54976731
75507868855078689TTCTC6GENICheterozygous54976733
75509650555096507AA--1GENIChomozygous53929101
75511010755110108TTTC6GENICheterozygous53929112
75512775355127755TC--16GENICheterozygous54976735
75515260055152601C-13GENIChomozygous53929123