chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2240587246240587247AAGT4GENICheterozygous59462339
2240587246240587247AAGTGTGT4GENICheterozygous60522922
2240587935240587936GA22GENIChomozygous59462340
2240588074240588075TTA23GENIChomozygous59462341
2240588099240588103TTTG----15GENIChomozygous60522923
2240588973240588974CT26GENIChomozygous59462343
2240589005240589006TA28GENIChomozygous59462344
2240589254240589255CT19GENIChomozygous59462345
2240590111240590112TC24GENIChomozygous59462346
2240590134240590135CG24GENIChomozygous59462347
2240590808240590809GA23GENIChomozygous59462348
2240590954240590955GA17GENICpossibly homozygous59462349
2240591183240591184CA11GENIChomozygous59462350
2240591794240591795GA25GENIChomozygous59462351
2240592169240592170CT15GENIChomozygous59462352
2240592407240592408CA26GENIChomozygous59462353
2240592529240592530CCACAA19GENIChomozygous59462354
2240592563240592564TG23GENIChomozygous59462355
2240592639240592640TC29GENIChomozygous59462356
2240592700240592701CCT26GENIChomozygous59462357
2240592743240592744TTG27GENIChomozygous59462358
2240593686240593687TG18GENIChomozygous59462360
2240596584240596586AC--10GENIChomozygous59462362
2240598760240598761GA9GENIChomozygous59462366
2240598950240598951A-5GENIChomozygous59462367
2240599775240599779ATAT----4GENIChomozygous59462368
2240601691240601692TC30GENIChomozygous59462369
2240604594240604595CCCAATCCA16GENIChomozygous59462370
2240605897240605898GC28GENIChomozygous59462371
2240610323240610324TA22GENIChomozygous59462376
2240610526240610527TC27GENIChomozygous59462377
2240610834240610835TC21GENIChomozygous59462378
2240611081240611082TA22GENIChomozygous60251262
2240611081240611082T-21GENIChomozygous60522927
2240596607240596615CACACACA--------2GENIChomozygous60551891