chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1128386605128386606TG48GENICheterozygous60850102
1128399390128399392GT--35GENICheterozygous60850103
1128401641128401642TG61GENICheterozygous60850104
1128404322128404323AAC9GENIChomozygous60850105
1128412038128412039GA52GENICpossibly homozygous60850106
1128412108128412114GTGTGT------38GENICheterozygous60850107
1128412110128412114GTGT----38GENICheterozygous60850108
1128412150128412154GTGT----31GENICheterozygous60850109
1128412191128412192GA12GENICheterozygous60850110
1128412257128412258AAT5GENICheterozygous60850111
1128412281128412282TA21GENICheterozygous60850112
1128412320128412321TTAG29GENICheterozygous60850113
1128412333128412334G-17GENICpossibly homozygous60850114
1128412333128412334GGT19GENIChomozygous60850115
1128412338128412339C-15GENIChomozygous60850116
1128413882128413883TTA8GENICheterozygous60850117