chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4898500948985010CG18GENIChomozygous45339518
X4898527048985271TTTG6GENICheterozygous45568813
X4898527148985273TG--6GENICheterozygous45508256
X4898656648986567GGA6GENIChomozygous45339519
X4898677148986772GGA17GENIChomozygous45298972
X4898896248988963AAC3GENIChomozygous45339520
X4898896348988964AAAAC3GENIChomozygous45339522
X4899056248990563GGCACA8GENICheterozygous45298973
X4899056248990563GGCACACACACA8GENICpossibly homozygous45667752
X4899126848991269AAGT8GENIChomozygous45667753
X4899189748991898GT4GENIChomozygous45339523
X4899199848991999GC7GENIChomozygous45339524
X4899205248992053GA9GENIChomozygous45339525
X4899460648994607GA14GENIChomozygous45339526
X4899484648994847AAT11GENIChomozygous45339527
X4899552448995525TC12GENIChomozygous45339528
X4899665048996651GGT3GENIChomozygous45298977
X4899789948997900TC9GENIChomozygous45339529
X4899806148998062TTA6GENIChomozygous45298978
X4899879448998795GA8GENIChomozygous45298979
X4899893648998937GA4GENIChomozygous45339530
X4899937648999378TT--2GENICheterozygous45298980
X4900003549000036AG1GENIChomozygous45339531
X4900042449000425TC6GENIChomozygous45339532
X4900056349000564CCT3GENIChomozygous45298982
X4900235149002352TC10GENIChomozygous45339533
X4900236249002363TC9GENIChomozygous45339534
X4900253049002531TC5GENIChomozygous45298983
X4900428249004283CA13GENIChomozygous45298984
X4900451749004518A-12GENIChomozygous45339535
X4900463749004638GGGTTT10GENIChomozygous45298985
X4900541349005414GC5GENIChomozygous45339536
X4900571849005726GTGTGTGT--------7GENIChomozygous45667754
X4900587449005875CCA9GENIChomozygous45298987
X4900589649005897GA7GENIChomozygous45339537
X4900603849006039CCTGAG4GENIChomozygous45298988
X4900620449006205A-6GENIChomozygous45128778
X4899937748999378T-2GENICheterozygous45128776
X4900622149006222A-6GENIChomozygous45339538
X4900714249007143TTAA2GENIChomozygous45339539
X4900750649007507AAAC10GENICheterozygous45339540