chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
177166363971663643CGGC----15GENIChomozygous724987534
177166364571663652GGAGTTC-------17GENIChomozygous724987535
177166370171663702AC21GENIChomozygous593888347
177166408971664090TTCACACACACACACACA2GENIChomozygous724987536
177166442171664422TTCTCTCACACACACACA12GENICheterozygous724987537
177166475271664755GGG---20GENIChomozygous724987539
177166502271665023A-21GENIChomozygous724987541
177166532171665322T-24GENICpossibly homozygous724987542
177166594671665947AG24GENIChomozygous593888348
177166633671666350TCTCTGTCTCTCTC--------------21GENIChomozygous724987543
177166637471666375AACACACT18GENICpossibly homozygous724987544
177166639771666398CCA24GENIChomozygous724987545
177166733571667336CT35GENIChomozygous593888349
177166778671667798GTGTGTGTGTGT------------16GENICheterozygous724987546
177166778871667798GTGTGTGTGT----------16GENICpossibly homozygous724987547
177166823371668234GA42GENIChomozygous594100967
177166926871669269GA22GENIChomozygous593888350
177166948271669483AC27GENIChomozygous593888351