chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134236660342366604GA15GENIChomozygous49939289
134236824042368241AG9GENIChomozygous49939291
134236865442368655AG6GENICheterozygous49939292
134236869342368694GA8GENICheterozygous49939293
134237330242373303GA15GENICpossibly homozygous49939296
134237417142374176CTGCA-----3GENIChomozygous49939297
134237440542374407TT--10GENIChomozygous49939298
134237457342374574AT9GENICheterozygous49736351
134237562842375631GGG---1GENIChomozygous49939301
134237599542375996CT19GENIChomozygous49736352
134237824242378243AG13GENIChomozygous49736354
134237900042379001TC7GENICpossibly homozygous49939305
134238189342381894GC4GENIChomozygous49736355
134238191742381918GA1GENIChomozygous49939306
134238209142382092AG14GENICpossibly homozygous49939307
134238336242383363GT17GENIChomozygous49939308
134238506842385069GA11GENICpossibly homozygous49939309
134238516242385163GA19GENIChomozygous49939310
134238547142385472GGAA5GENIChomozygous49736360
134238625942386260GC15GENIChomozygous49939311
134238695042386951CT16GENICpossibly homozygous49939315
134238699242386993AG12GENICheterozygous49736364
134238702242387023AC12GENICheterozygous49736365
134238762742387628TA4GENIChomozygous49939316
134238764542387646TA7GENICpossibly homozygous49939317
134238892142388922TC2GENIChomozygous49736367
134238999842389999AG11GENIChomozygous49736369
134239025442390255TC15GENIChomozygous49736370
134239062242390623G-2GENIChomozygous49736371
134239066342390664G-1GENIChomozygous49736373
134239066742390668G-1GENIChomozygous49736374
134239069442390695TC9GENIChomozygous49939321
134239075342390754C-1GENIChomozygous49736375
134239109842391099A-2GENIChomozygous49736378
134239149342391494CCT4GENICheterozygous49939323
134239264142392642AG13GENIChomozygous49736381
134239281142392812GGT12GENIChomozygous49736383
134239350442393505AT9GENICpossibly homozygous49736386