chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2240587246240587247AAGTGTGT2GENIChomozygous60522922
2240587935240587936GA25GENIChomozygous59462340
2240588074240588075TTA36GENIChomozygous59462341
2240588099240588103TTTG----19GENIChomozygous60522923
2240588973240588974CT28GENIChomozygous59462343
2240589005240589006TA29GENIChomozygous59462344
2240589254240589255CT27GENIChomozygous59462345
2240590111240590112TC28GENIChomozygous59462346
2240590134240590135CG24GENIChomozygous59462347
2240590808240590809GA25GENIChomozygous59462348
2240590954240590955GA29GENIChomozygous59462349
2240591183240591184CA29GENIChomozygous59462350
2240591794240591795GA28GENIChomozygous59462351
2240592169240592170CT27GENIChomozygous59462352
2240592407240592408CA22GENIChomozygous59462353
2240592529240592530CCACAA16GENIChomozygous59462354
2240592563240592564TG25GENIChomozygous59462355
2240592639240592640TC23GENIChomozygous59462356
2240592700240592701CCT27GENIChomozygous59462357
2240592743240592744TTG31GENIChomozygous59462358
2240593686240593687TG28GENIChomozygous59462360
2240596584240596586AC--15GENIChomozygous59462362
2240598760240598761GA15GENIChomozygous59462366
2240598950240598951A-15GENIChomozygous59462367
2240599775240599779ATAT----5GENIChomozygous59462368
2240601691240601692TC25GENIChomozygous59462369
2240604594240604595CCCAATCCA23GENIChomozygous59462370
2240605897240605898GC22GENIChomozygous59462371
2240610323240610324TA21GENIChomozygous59462376
2240610526240610527TC20GENIChomozygous59462377
2240610834240610835TC26GENIChomozygous59462378
2240611081240611082TA20GENIChomozygous60251262
2240611081240611082T-18GENIChomozygous60522927
2240595356240595359AAA---7GENICheterozygous60551890
2240596607240596615CACACACA--------5GENIChomozygous60551891