chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171006637171006638AAG13GENIChomozygous60941889
1171006649171006650AAG13GENICpossibly homozygous60941891
1171006678171006679AAGGG1GENIChomozygous62173533
1171006679171006680AAAGG1GENIChomozygous62173535
1171006682171006683AAGGGAAGGGAAG1GENIChomozygous62173537
1171009499171009500GA19GENICpossibly homozygous60941897
1171008253171008254GA14GENIChomozygous61960663
1171008303171008304CCT10GENIChomozygous61960664
1171009510171009511TTA17GENIChomozygous61555237
1171008279171008280A-7GENIChomozygous61784615
1171010074171010075AG9GENIChomozygous60941901
1171010106171010107TC9GENIChomozygous61960666
1171010251171010252GA19GENIChomozygous60941902
1171010468171010474AAAAAA------12GENIChomozygous61309815
1171010621171010622GA25GENIChomozygous60941905
1171010794171010795CT30GENIChomozygous61555240
1171011151171011152CT24GENIChomozygous61960667
1171011216171011217GT28GENIChomozygous61960668
1171013457171013458TTAAAAA3GENIChomozygous61555246
1171014031171014032TC22GENIChomozygous61960669
1171014042171014043CA18GENIChomozygous61960670
1171014231171014232AG17GENIChomozygous61555248
1171014391171014392TC19GENIChomozygous61555249
1171015370171015371AC14GENIChomozygous61960671
1171015885171015886CT20GENIChomozygous61555251