chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55924864859248649TG20GENIChomozygous137479431
55924978359249784AG13GENIChomozygous137479432
55925063759250638CT17GENIChomozygous137479433
55925078959250790GA13GENIChomozygous143225791
55925079959250800CT12GENIChomozygous143225792
55925142059251421CT14GENIChomozygous143225793
55925389859253899CA17GENIChomozygous143225794
55925428159254282CT19GENIChomozygous143225795
55925480559254806AG20GENIChomozygous137479436
55925545459255455CA17GENIChomozygous137479437
55925603459256034G8GENIChomozygous143179997
55925738759257387A6GENIChomozygous143179998
55925770559257706AG14GENIChomozygous137479438
55925797159257972GA13GENIChomozygous143225796
55925827159258271A7GENICpossibly homozygous137310913
55925828059258281TA9GENICpossibly homozygous137479440
55925828459258285TA9GENICpossibly homozygous143225797
55925837259258372G8GENICheterozygous137310914
55926079459260795AT16GENIChomozygous137479442
55926119359261194CG23GENIChomozygous137479443
55926145159261452AG14GENIChomozygous137479444
55926180559261806CT19GENIChomozygous137479445
55926185259261853CA10GENIChomozygous137479446
55926197259261973AG12GENIChomozygous137479447
55926222059262220T12GENIChomozygous137310915
55926282459262825C20GENIChomozygous137310916
55926285459262855TC18GENIChomozygous137479448
55926323659263237CT20GENIChomozygous137479449
55926341259263417GGACA23GENIChomozygous137310917
55926439459264395GA19GENIChomozygous143225798
55926519059265191GT16GENIChomozygous143225799