chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76211421762114218CT18GENICpossibly homozygous53934465
76211595162115952T-14GENIChomozygous53934466
76211758362117584AG8GENICheterozygous53934467
76211804162118042TG14GENICpossibly homozygous53934468
76211914162119142TA30GENICpossibly homozygous53934469
76212219562122196TA6GENIChomozygous53934471
76212234562122346C-7GENICpossibly homozygous53934472
76212235762122358TC9GENICpossibly homozygous53934473
76212419762124198A-1GENIChomozygous53934475
76212582062125821TC18GENICpossibly homozygous53934476
76212927762129278CT8GENICpossibly homozygous53934481
76213084562130846AG9GENICpossibly homozygous53934482
76213237062132371CT4GENICheterozygous53934486
76213392662133927AG13GENIChomozygous53934487
76213445162134452TC17GENIChomozygous53934488
76213546462135465GA20GENIChomozygous53934490
76213547662135477GC14GENIChomozygous53934491
76213566562135666T-17GENIChomozygous53934492
76213574962135750GT18GENICpossibly homozygous53934493
76212837762128387TCGGGTGTGC----------7GENIChomozygous55311312
76213188262131883AC5GENICheterozygous55311315
76213186862131869A-1GENIChomozygous55141854
76213732962137330TC17GENIChomozygous53934495
76213956662139567A-4GENIChomozygous53934497
76213957662139577AAG3GENIChomozygous53934498
76214045362140454TC10GENIChomozygous53934499
76214158262141583A-3GENIChomozygous53934503
76214232662142327TTG10GENICpossibly homozygous53934504
76214313962143140TC15GENICpossibly homozygous53934505
76214325562143256AAC2GENICheterozygous53934509
76214326662143267CA2GENIChomozygous55025590
76214917162149172AACACT16GENICheterozygous53934511