chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96713178067131781GA26GENIChomozygous117711303
96713324967133250CT46GENIChomozygous117711305
96713347867133479CT34GENIChomozygous117711307
96713578467135785CG17GENIChomozygous117370957
96713579667135797AG17GENIChomozygous117711309
96713615967136160TC48GENIChomozygous117370959
96713672967136730GT50GENIChomozygous117370963
96713692767136928GA31GENIChomozygous120340617
96713784667137847TC22GENIChomozygous117370965
96713797367137974TC19GENIChomozygous120340618
96713826267138263AG42GENIChomozygous117370967
96713877767138778TG28GENIChomozygous117370971
96713922567139226GA18GENIChomozygous117370973
96714115867141159TC19GENIChomozygous117370981
96714182767141828CA25GENIChomozygous117370993
96714185167141852AG23GENIChomozygous117582770
96714185267141853GA23GENIChomozygous117582772
96714187867141879TC22GENIChomozygous117370995
96714189967141900TC24GENIChomozygous117582776
96714359167143592GA18GENIChomozygous120395243
96714597467145975TC26GENIChomozygous117371005
96714737867147379CT27GENIChomozygous120340619
96714977567149776AC7GENICpossibly homozygous117371017
96715336967153370CT15GENIChomozygous120340620
96715440067154401CT17GENIChomozygous117371053
96715739267157393GA20GENIChomozygous117371063
96715959767159598GA9GENIChomozygous117550862
96715982467159825GA9GENIChomozygous117550864
96715991367159914AG10GENIChomozygous117371069
96716076267160763AG14GENIChomozygous117371073
96716788167167882GC16GENIChomozygous120395245
96716807567168076CT19GENIChomozygous117550870
96716830967168310TC21GENIChomozygous117550872
96716875867168759GC9GENIChomozygous117550874
96716898167168982GA14GENIChomozygous117550876