chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48465050284650503AG10GENIChomozygous112758248
48465063284650633TG26GENIChomozygous112758250
48465085684650857CT13GENICheterozygous112758252
48465134784651348TC18GENIChomozygous112758254
48465141484651415CA11GENIChomozygous119278747
48465141584651416AG11GENIChomozygous112758256
48465154984651550GA22GENIChomozygous112758258
48465189784651898GA24GENIChomozygous112758260
48465238984652390TA11GENIChomozygous112758264
48465296584652966CT16GENIChomozygous112758266
48465301284653013TC21GENIChomozygous112758268
48465307884653079CT7GENIChomozygous112758270
48465308584653086TA10GENIChomozygous112758272
48465362784653628GA14GENIChomozygous112758274
48465395484653955CT7GENIChomozygous112758276
48465400984654010GA4GENIChomozygous126050401
48465401084654011TA17GENICheterozygous119278749
48465467584654676AG11GENICheterozygous112758278
48465471484654715AG16GENIChomozygous112758280
48465492484654925AG14GENIChomozygous112758282
48465503184655032AG11GENIChomozygous112758284
48465507284655073TC8GENIChomozygous112758286
48465512984655130TC10GENIChomozygous112758288
48465564784655648AG27GENIChomozygous112758290
48465569484655695AG16GENIChomozygous112758292
48465604084656041GA14GENIChomozygous112758298
48465614184656142CT12GENIChomozygous112758300