chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219099213219099214AG17GENIChomozygous61593499
1219099560219099561GT21GENIChomozygous62101042
1219104584219104585TC21GENICpossibly homozygous61593500
1219105217219105218GA31GENICpossibly homozygous62101043
1219106773219106774AG13GENICheterozygous62101044
1219107257219107258GA12GENICpossibly homozygous62101045
1219112574219112586CACACACACACC------------7GENICheterozygous62101046
1219113134219113135GGT1GENIChomozygous62101047
1219114307219114308AG29GENICpossibly homozygous61593528
1219114929219114930CT21GENICpossibly homozygous62101048
1219118046219118164CTCAGCCCCACATTCTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTCCTAGGGAAGCGCTCTACCACTGAGCTAAATCCCCAACCC----------------------------------------------------------------------------------------------------------------------23GENICheterozygous62101049
1219118369219118370CT10GENIChomozygous62101050
1219119522219119523AT11GENICpossibly homozygous62101051
1219124043219124044CT24GENICpossibly homozygous62101052
1219127277219127278TG7GENIChomozygous61593570
1219128314219128315TC25GENIChomozygous61593574
1219128553219128554GA30GENICpossibly homozygous62101053
1219129721219129722CCAA7GENICpossibly homozygous61593578
1219130308219130309CCA28GENIChomozygous61593579
1219132609219132610TG16GENIChomozygous61593581