chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171008303171008304CCT2GENIChomozygous61960664
1171009499171009500GA6GENIChomozygous60941897
1171009510171009511TTA1GENIChomozygous61555237
1171009926171009927AG2GENICheterozygous62544992
1171010106171010107TC1GENIChomozygous61960666
1171010621171010622GA12GENICpossibly homozygous60941905
1171010794171010795CT19GENIChomozygous61555240
1171011151171011152CT19GENICheterozygous61960667
1171011216171011217GT14GENIChomozygous61960668
1171014031171014032TC3GENIChomozygous61960669
1171014042171014043CA2GENIChomozygous61960670
1171014231171014232AG19GENICpossibly homozygous61555248
1171014391171014392TC13GENIChomozygous61555249
1171015370171015371AC15GENICheterozygous61960671
1171015885171015886CT22GENICpossibly homozygous61555251