chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177448704177448705CCTTTCTTTTCTTTTCT6GENIChomozygous61561591
1177448861177448862TC12GENIChomozygous60968909
1177450079177450080TC29GENIChomozygous60968912
1177452556177452580AGAGAGAGAGAGAGAGAGAGAGAG------------------------22GENICpossibly homozygous61561592
1177454699177454700TG22GENIChomozygous60968914
1177455131177455132GA31GENIChomozygous61561593
1177455652177455653GT19GENIChomozygous60968916
1177455697177455698AG33GENIChomozygous60968918
1177455702177455703TG32GENIChomozygous60968920
1177458155177458156AG35GENIChomozygous60968922
1177458696177458697GA14GENIChomozygous60968924
1177460313177460314AC22GENIChomozygous60968926
1177460604177460605CCTTCCCATGGTT14GENIChomozygous60968928
1177460937177460938C-32GENIChomozygous61561594
1177461870177461871T-11GENICheterozygous61561595
1177462194177462195TTTCTCTCTGAA30GENIChomozygous60968933
1177462551177462552CT51GENIChomozygous60968935
1177462667177462668GA42GENIChomozygous60968937
1177464998177464999TC27GENIChomozygous60968939
1177465707177465708TC38GENIChomozygous60968941
1177466215177466216GC10GENIChomozygous60968943
1177466239177466240GGAAAAAAAAAAAAAA4GENIChomozygous62178591
1177466749177466750AG34GENIChomozygous60968947
1177466998177466999AG28GENIChomozygous60968949
1177467619177467620TG25GENIChomozygous60968951
1177468215177468217AC--23GENICpossibly homozygous62178595
1177469064177469065CT28GENIChomozygous60968957
1177469979177469980AG32GENIChomozygous60968959
1177468211177468217ACACAC------23GENICheterozygous62343691