chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1126233893126233894GC12GENIChomozygous61753425
1126234027126234028GC15GENIChomozygous60843590
1126234298126234299GA17GENIChomozygous60843591
1126235981126235982A-10GENIChomozygous60843594
1126236111126236112TC14GENIChomozygous60843595
1126236190126236191GT11GENIChomozygous61515562
1126237389126237390GC14GENIChomozygous60843597
1126237597126237598CCCCAT9GENIChomozygous62623263
1126241478126241479TC8GENIChomozygous60843602
1126241682126241683GA13GENIChomozygous60843603
1126241837126241838TC15GENIChomozygous60843605
1126241939126241940CA9GENIChomozygous60843606
1126241972126241973CT9GENIChomozygous61515566
1126242057126242058AT13GENIChomozygous60843607
1126242859126242860CA19GENIChomozygous60843611
1126242866126242867TC18GENIChomozygous60843612
1126242954126242955GC11GENIChomozygous60843616
1126242966126242967TC10GENIChomozygous60843617
1126243065126243066CA13GENIChomozygous61515568
1126243069126243072CTT---12GENIChomozygous62623264
1126243178126243179TC12GENIChomozygous62295661
1126243229126243230TA11GENIChomozygous62623265
1126243618126243619TTTTG12GENIChomozygous60843618
1126245306126245307TA16GENIChomozygous60843621
1126245998126245999T-15GENIChomozygous60843624
1126246695126246696GA11GENIChomozygous62623266
1126250831126250832TA18GENIChomozygous60843642
1126252008126252009GA16GENIChomozygous62623269
1126258124126258125AC14GENIChomozygous61515576
1126262173126262174TC9GENIChomozygous60843683
1126270329126270330TC33GENIChomozygous62086907
1126270399126270400AG28GENIChomozygous60843718
1126270560126270561CA12GENIChomozygous60843719
1126270574126270575AG13GENIChomozygous62623270
1126274186126274187TC8GENIChomozygous61753465
1126278749126278750GA8GENIChomozygous62623271
1126282090126282091TC10GENIChomozygous60843747
1126243028126243029CT12GENIChomozygous62867238