chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1208958224208958225GC46GENIChomozygous61588034
1208958791208958792TC45GENIChomozygous61588035
1208958896208958897CT25GENICpossibly homozygous61588036
1208959737208959738TC29GENIChomozygous61588037
1208960481208960482GA20GENICheterozygous61588038
1208960804208960805AG43GENIChomozygous61588039
1208962915208962916TC31GENIChomozygous61588040
1208963024208963025TC53GENICpossibly homozygous61588041
1208963970208963971CCA14GENICpossibly homozygous61588042
1208964072208964073TC21GENICpossibly homozygous61588043
1208964228208964229CT39GENIChomozygous61588044
1208965586208965587AT41GENIChomozygous61588045
1208965715208965716AG36GENIChomozygous61588046
1208965782208965783CCTCTG38GENIChomozygous61588047
1208966298208966299TC54GENIChomozygous61588048
1208966567208966568GA45GENIChomozygous61588049
1208966586208966587CT43GENIChomozygous61588050
1208966978208966979CT40GENIChomozygous61588051
1208967190208967191TC50GENIChomozygous61588052
1208967272208967273GC55GENIChomozygous61588053
1208967357208967358TC41GENIChomozygous61588054
1208967364208967365A-34GENIChomozygous61588055
1208967770208967771GGGAC7GENIChomozygous61588056
1208967826208967827GC25GENIChomozygous61588057
1208968024208968025AT22GENICheterozygous61588058
1208968028208968029AT21GENICheterozygous61588059
1208968032208968033AC21GENICheterozygous61588060
1208968052208968053AT19GENIChomozygous61588061
1208968056208968057CT20GENIChomozygous61588062
1208968528208968529GC34GENICpossibly homozygous61588063
1208968587208968588TG33GENIChomozygous61588064
1208968609208968610AG33GENIChomozygous61588065
1208968644208968645C-36GENIChomozygous61588066
1208968709208968710AC36GENIChomozygous61588067
1208968726208968727AG35GENIChomozygous61588068
1208968913208968914AG34GENIChomozygous61588069
1208973836208973837GGA15GENICheterozygous61588070
1208974015208974016CCA28GENIChomozygous61070531
1208974022208974023CCA31GENIChomozygous61070532