chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2240587246240587247AAGT7GENICheterozygous59462339
2240587935240587936GA25GENIChomozygous59462340
2240588074240588075TTA18GENIChomozygous59462341
2240588095240588099TTTG----10GENIChomozygous59462342
2240588973240588974CT20GENIChomozygous59462343
2240589005240589006TA23GENIChomozygous59462344
2240589254240589255CT22GENIChomozygous59462345
2240590111240590112TC15GENIChomozygous59462346
2240590134240590135CG19GENIChomozygous59462347
2240590808240590809GA21GENIChomozygous59462348
2240590954240590955GA20GENIChomozygous59462349
2240591183240591184CA13GENIChomozygous59462350
2240591794240591795GA20GENIChomozygous59462351
2240592169240592170CT18GENIChomozygous59462352
2240592407240592408CA24GENIChomozygous59462353
2240592529240592530CCACAA22GENIChomozygous59462354
2240592563240592564TG17GENIChomozygous59462355
2240592639240592640TC18GENIChomozygous59462356
2240592700240592701CCT14GENIChomozygous59462357
2240592743240592744TTG14GENIChomozygous59462358
2240593686240593687TG26GENICpossibly homozygous59462360
2240595357240595359AA--4GENICheterozygous59462361
2240596584240596586AC--10GENIChomozygous59462362
2240596601240596603TG--16GENICheterozygous59462363
2240596603240596611CACACACA--------6GENICheterozygous59462364
2240597805240597807TG--9GENICheterozygous59462365
2240598760240598761GA22GENIChomozygous59462366
2240598950240598951A-14GENIChomozygous59462367
2240599775240599779ATAT----1GENIChomozygous59462368
2240601691240601692TC15GENIChomozygous59462369
2240604594240604595CCCAATCCA19GENIChomozygous59462370
2240605897240605898GC22GENIChomozygous59462371
2240608191240608192GA26GENIChomozygous59462372
2240608402240608403AC20GENICpossibly homozygous59462373
2240610323240610324TA6GENIChomozygous59462376
2240610526240610527TC29GENIChomozygous59462377
2240610834240610835TC19GENIChomozygous59462378
2240611079240611080T-13GENIChomozygous59462379