chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148233785382337854TC40GENIChomozygous113603784
148233918482339185AG51GENIChomozygous113603785
148234263282342633CA39GENICpossibly homozygous113603786
148234461082344611GA43GENIChomozygous113603787
148234461182344612TA43GENIChomozygous113603788
148234505982345060TG26GENIChomozygous113603789
148234525082345251TC40GENIChomozygous113603790
148234844882348449AG27GENIChomozygous113603791
148234552082345520A13GENIChomozygous133434003
148234791282347912T35GENIChomozygous129178122
148234791982347919G36GENIChomozygous129178123
148234792582347925G35GENIChomozygous129178124
148234793882347938T29GENIChomozygous129178125
148234978082349780GGGACGAGAGTTTCATACAGGAGACCCTCGACTAAACAGGAACCTGGCGCGGCCTCTTTGGAGGACCGACATCAACTAGGTCAGACCGAGACCACGGGCAGGCCGGCCTGCAATGCCCAGTACGCCGGTTCCAGTCCTGTCTAGGAGGCTAGGCCCATCCCTTAGCTCAGAAAAGA39GENICpossibly homozygous129178126