chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204481207744812078AG26GENIChomozygous45636869
204481222744812228T-19GENICpossibly homozygous45924788
204481267244812673GA21GENIChomozygous45993633
204481470944814710TC23GENIChomozygous45636872
204481486044814861TTACCCGCTGAACGC21GENIChomozygous45993634
204481553344815535AG--22GENIChomozygous45993635
204481746244817463AAAGGGGCTGGGG8GENIChomozygous45903752
204481759144817592CCAAAAAA5GENIChomozygous45875036
204481787844817879CA28GENICpossibly homozygous45993636
204481837844818379GA18GENICheterozygous45636879
204481762344817624AG4GENIChomozygous45575511
204481911944819136ACGGCAACCGCGCTCTG-----------------24GENIChomozygous45993637
204481970844819709TG24GENIChomozygous45636880
204482062044820621AG33GENIChomozygous45636882
204482428244824283TC36GENIChomozygous45636884
204482548244825483CT30GENIChomozygous45636885
204482599544825996CT23GENICpossibly homozygous45830609
204482623344826234AG18GENIChomozygous45993638
204482630244826303CG16GENICpossibly homozygous45764781
204482647744826479AA--6GENIChomozygous45636888
204482654844826549CT23GENIChomozygous45636889
204482671844826719GA19GENIChomozygous45636890
204482691644826917T-13GENIChomozygous45993639
204482693344826934TTTTG12GENIChomozygous45993640
204482805844828059AG34GENICpossibly homozygous45993641
204482946144829462AATTT29GENIChomozygous45636894
204482946344829464AATTGT28GENIChomozygous45636896
204482977544829776AG20GENIChomozygous45636897
204483050644830507GA22GENICpossibly homozygous45993642
204483135244831353TC15GENIChomozygous45993643
204483157444831575G-11GENIChomozygous45764790
204483184344831844TC18GENIChomozygous45636901
204483201744832028AAAACAAAACA-----------14GENIChomozygous45993644
204483220744832212ACAAC-----16GENIChomozygous45830617
204483267944832680CCA24GENICpossibly homozygous45764797
204483408844834089CT27GENICheterozygous45636907
204483418244834183CT32GENIChomozygous45830619
204483448844834489CT24GENIChomozygous45636908
204483515844835159TC13GENIChomozygous45636909