chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8131978950131978951AG31GENIChomozygous52900379
8131979290131979291CT23GENICpossibly homozygous52900381
8131980128131980129T-1GENIChomozygous52900382
8131980221131980222TC18GENIChomozygous52900384
8131980324131980325AC27GENIChomozygous52900386
8131980619131980620GGCACA18GENIChomozygous53583356
8131981631131981633CC--7GENIChomozygous53581062
8131982553131982554A-5GENIChomozygous52900394
8131983073131983074TC7GENICpossibly homozygous52900396
8131983657131983665TGTGTCTG--------5GENIChomozygous52900398
8131983732131983733GC10GENIChomozygous52900400
8131983799131983808CTCTAGTTC---------2GENIChomozygous52900402
8131983919131983920TC13GENICpossibly homozygous52900404
8131984499131984509ACAGAGAGAG----------2GENIChomozygous52900408
8131984693131984694T-9GENIChomozygous52900410
8131984694131984695TA8GENIChomozygous53583357
8131984935131984936T-14GENIChomozygous52900412
8131985166131985167CA23GENICpossibly homozygous52900414
8131985271131985272TG17GENIChomozygous52900416
8131985640131985641TC6GENICheterozygous53583358
8131985641131985642GA6GENICheterozygous53583359
8131985851131985852CT9GENIChomozygous52900422
8131985901131985902TC17GENIChomozygous52900424
8131986445131986446CT22GENICheterozygous52900426
8131986481131986482CT18GENICpossibly homozygous52900428
8131986730131986731TC8GENIChomozygous52900430
8131987352131987353GT26GENIChomozygous52900432
8131990473131990474TG13GENIChomozygous52900434
8131991273131991274CT7GENICheterozygous52900438