chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1684175168417518GG--2GENICheterozygous47722684
1684175258417526GA4GENICheterozygous47901443
1684195368419537GT25GENIChomozygous47605552
1684195388419539TG25GENIChomozygous47605553
1684239158423916GA26GENIChomozygous47798471
1684246098424610CCCTGGTTTGGTTA32GENIChomozygous47260003
1684260118426012TTGGA33GENIChomozygous47260005
1684266458426646AG17GENIChomozygous47260007
1684267508426751G-25GENIChomozygous47722702
1684267928426793AG28GENIChomozygous47722704
1684268058426806GC23GENIChomozygous47784831
1684273168427317GGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTC10GENIChomozygous47941701
1684274938427494TTGTGTGTGTGTGTCC28GENICpossibly homozygous48136936
1684248608424861CT20GENICpossibly homozygous48136933
1684267978426798AC28GENIChomozygous48136934
1684268018426802CA27GENIChomozygous48136935
1684273758427377TG--5GENIChomozygous48084478
1684279098427910GA40GENIChomozygous48136937
1684281618428162GA27GENIChomozygous47881051
1684285718428572TC19GENIChomozygous47260036
1684286088428609AAGGCCTGAGAGGCGCAGGGGCCTGAGAGGCGCAGG8GENIChomozygous47901453
1684286618428662TTC1GENIChomozygous47881052
1684286668428667TG4GENIChomozygous47901455
1684300398430040CT28GENIChomozygous47881053
1684301848430185CT23GENIChomozygous47881054
1684333238433324AG29GENIChomozygous47260048
1684333528433353CT28GENIChomozygous47881056
1684350868435087GA27GENIChomozygous47881057
1684352838435284CT25GENIChomozygous48136938
1684360778436078CT33GENIChomozygous48136939
1684368548436855GA18GENIChomozygous48136940
1684368788436879CT14GENIChomozygous47260053
1684373478437348G-21GENICpossibly homozygous48136941
1684373498437350TG21GENICpossibly homozygous48136942
1684373898437390GC26GENICpossibly homozygous48136943
1684385588438559GA13GENICheterozygous47722747
1684385628438563TC12GENICheterozygous47722748
1684394108439411AATG2GENIChomozygous47986626