chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105596690255966903G-8GENICpossibly homozygous51459950
105596690755966908A-7GENICpossibly homozygous52460609
105596837655968377GGAAAAAA17GENICheterozygous52319076
105596952955969533CACA----18GENIChomozygous51459952
105597007155970072TC15GENIChomozygous51654080
105597140755971408A-10GENIChomozygous51459955
105597235655972357TC21GENICpossibly homozygous51654086
105597574355975744A-19GENIChomozygous51459958
105597613355976134CCTT8GENICpossibly homozygous51459959
105597628455976285CCA28GENIChomozygous51654090
105597665755976658T-13GENIChomozygous51654092
105597686055976861GGT8GENICheterozygous51654094
105597701655977017AG25GENICpossibly homozygous51654098
105597771155977712CT15GENIChomozygous52058872
105596837755968380AAA---17GENICpossibly homozygous52058868
105597017255970173T-7GENICheterozygous51890869
105597132555971326CCA1GENIChomozygous51890872
105597487455974876AG--8GENICheterozygous52723928
105597488355974884TTTTTTTA9GENICheterozygous52723931
105597951055979511CT21GENICpossibly homozygous51654099
105598009355980094T-11GENICheterozygous51654107
105598051255980513TTAAC22GENIChomozygous51654109
105598053355980534TC31GENIChomozygous51654111
105598053655980537TC32GENICpossibly homozygous52058874
105598117455981175AG30GENIChomozygous51654115
105598172255981725TTT---4GENICheterozygous51986649
105598265655982657T-22GENIChomozygous52058876