chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48465050284650503AG11GENIChomozygous112758248
48465063284650633TG24GENIChomozygous112758250
48465085684650857CT19GENIChomozygous112758252
48465134784651348TC20GENIChomozygous112758254
48465141584651416AG20GENIChomozygous112758256
48465154984651550GA20GENIChomozygous112758258
48465189784651898GA17GENIChomozygous112758260
48465296584652966CT6GENIChomozygous112758266
48465307884653079CT17GENIChomozygous112758270
48465308584653086TA14GENIChomozygous112758272
48465324384653244CA20GENIChomozygous119435538
48465362784653628GA23GENIChomozygous112758274
48465395484653955CT22GENIChomozygous112758276
48465401084654011TA18GENIChomozygous119278749
48465465484654655CG32GENIChomozygous119278751
48465467584654676AG31GENIChomozygous112758278
48465471484654715AG23GENIChomozygous112758280
48465492484654925AG15GENIChomozygous112758282
48465503184655032AG26GENIChomozygous112758284
48465507284655073TC20GENIChomozygous112758286
48465512984655130TC18GENIChomozygous112758288
48465564784655648AG25GENIChomozygous112758290
48465569484655695AG31GENIChomozygous112758292
48465596684655967GA22GENIChomozygous112758294
48465596784655968GA21GENIChomozygous112758296
48465604084656041GA20GENIChomozygous112758298
48465614184656142CT11GENIChomozygous112758300
48465624284656243GA21GENIChomozygous112758302
48465638284656383CT17GENIChomozygous112758304
48465638484656385TC17GENIChomozygous112758306
48465647384656474TC15GENIChomozygous112758308
48465653484656535TG11GENIChomozygous112758310