chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55924473059244750ACTGCCTTCAGTGGTCTCTT22GENIChomozygous137310909
55924475459244757CCA22GENIChomozygous137310910
55924864859248649TG19GENIChomozygous137479431
55924978359249784AG14GENIChomozygous137479432
55925042559250426G8GENIChomozygous137310911
55925063759250638CT16GENIChomozygous137479433
55925092159250922AT13GENIChomozygous137479434
55925157859251579CT20GENIChomozygous137479435
55925480559254806AG24GENIChomozygous137479436
55925545459255455CA23GENIChomozygous137479437
55925603959256040A14GENIChomozygous137310912
55925770559257706AG21GENIChomozygous137479438
55925788059257881TA22GENIChomozygous137479439
55925827159258271A8GENIChomozygous137310913
55925828059258281TA9GENIChomozygous137479440
55925837259258372G4GENIChomozygous137310914
55925856559258566TA19GENIChomozygous137479441
55926079459260795AT20GENIChomozygous137479442
55926119359261194CG29GENIChomozygous137479443
55926145159261452AG17GENIChomozygous137479444
55926180559261806CT22GENIChomozygous137479445
55926185259261853CA20GENIChomozygous137479446
55926197259261973AG14GENIChomozygous137479447
55926222059262220T22GENICpossibly homozygous137310915
55926282459262825C20GENIChomozygous137310916
55926285459262855TC19GENIChomozygous137479448
55926323659263237CT18GENIChomozygous137479449
55926341259263417GGACA19GENIChomozygous137310917
55926543259265433TC21GENIChomozygous137479450