chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2240587246240587247AAGT12GENICheterozygous59462339
2240587246240587247AAGTGTGT12GENICheterozygous60522922
2240587935240587936GA19GENIChomozygous59462340
2240588074240588075TTA11GENIChomozygous59462341
2240588099240588103TTTG----9GENIChomozygous60522923
2240588973240588974CT21GENIChomozygous59462343
2240589005240589006TA25GENIChomozygous59462344
2240589254240589255CT18GENIChomozygous59462345
2240590111240590112TC18GENIChomozygous59462346
2240590134240590135CG19GENIChomozygous59462347
2240590808240590809GA17GENIChomozygous59462348
2240590954240590955GA31GENIChomozygous59462349
2240591183240591184CA20GENIChomozygous59462350
2240591794240591795GA35GENIChomozygous59462351
2240592169240592170CT9GENIChomozygous59462352
2240592407240592408CA15GENIChomozygous59462353
2240592529240592530CCACAA19GENIChomozygous59462354
2240592563240592564TG19GENIChomozygous59462355
2240592639240592640TC17GENIChomozygous59462356
2240592700240592701CCT12GENIChomozygous59462357
2240592743240592744TTG13GENIChomozygous59462358
2240593686240593687TG25GENIChomozygous59462360
2240596584240596586AC--15GENIChomozygous59462362
2240598760240598761GA15GENIChomozygous59462366
2240598950240598951A-14GENIChomozygous59462367
2240599775240599779ATAT----1GENIChomozygous59462368
2240601691240601692TC30GENIChomozygous59462369
2240604594240604595CCCAATCCA25GENIChomozygous59462370
2240605897240605898GC25GENIChomozygous59462371
2240610323240610324TA13GENIChomozygous59462376
2240610526240610527TC17GENIChomozygous59462377
2240610834240610835TC25GENIChomozygous59462378
2240611081240611082TA12GENIChomozygous60251262
2240611081240611082T-12GENIChomozygous60522927
2240595356240595359AAA---4GENICheterozygous60551890
2240596607240596615CACACACA--------8GENICpossibly homozygous60551891