chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38084590680845907AG30GENICheterozygous111635872
38085138580851386TC34GENIChomozygous111635873
38085291780852918GA38GENIChomozygous111635874
38085328580853286AC49GENIChomozygous111635875
38085860480858605TC48GENIChomozygous111635876
38086041480860415GT36GENICpossibly homozygous111635877
38086119280861193CA25GENIChomozygous111635878
38086174380861744GT39GENIChomozygous111635879
38086188180861882AC22GENICpossibly homozygous111635880
38086223180862232CA40GENICpossibly homozygous111635881
38086454380864544CT47GENICpossibly homozygous111635882
38086660980866610GA52GENIChomozygous111635883
38087061180870612TC56GENIChomozygous111635884
38087284880872849AG26GENIChomozygous111635885
38087368380873684GC14GENICpossibly homozygous111635886
38087534680875347GT45GENICpossibly homozygous111635887
38087993980879940AG44GENIChomozygous111635888
38087994280879943CT43GENIChomozygous111635889
38088063280880633GC52GENIChomozygous111635890
38088319280883193CT37GENIChomozygous111635891
38088334980883350TC35GENIChomozygous111635892
38088446280884463CT55GENIChomozygous111635893
38088576580885766GT37GENICpossibly homozygous111635894
38088596780885968CA26GENICpossibly homozygous111635895
38088610280886103GC28GENICpossibly homozygous111635896
38088614280886143AG27GENIChomozygous111635897