chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2181296089181296090GA52GENIChomozygous110156018
2181296158181296159GA41GENIChomozygous110156019
2181296238181296239AG27GENIChomozygous110156020
2181296697181296698CA22GENIChomozygous110156021
2181296720181296721CT23GENICpossibly homozygous110156022
2181296833181296834GA20GENIChomozygous110156023
2181297156181297157AT45GENICheterozygous110156024
2181297239181297240GA15GENIChomozygous110156025
2181297369181297370GA33GENIChomozygous110156026
2181297451181297452AG51GENIChomozygous110156027
2181297796181297797CA57GENICpossibly homozygous110156028
2181297843181297844TC62GENIChomozygous110156029
2181297869181297870CA47GENICpossibly homozygous110156030
2181297881181297882GA47GENIChomozygous110156031
2181297884181297885CT44GENICpossibly homozygous110156032
2181297936181297937GA45GENIChomozygous110156033
2181297962181297963CA44GENICheterozygous110156034
2181298493181298494GA57GENICpossibly homozygous110156035
2181298516181298517GA57GENICheterozygous110156036
2181298584181298585TC63GENIChomozygous110156037
2181298605181298606GA56GENICheterozygous110156038
2181298790181298791CA52GENICheterozygous110156039
2181298908181298909TC57GENICheterozygous110156040
2181298914181298915CT52GENICheterozygous110156041
2181298966181298967GT41GENICpossibly homozygous110156042
2181298968181298969GA40GENIChomozygous110156043
2181298991181298992CT35GENIChomozygous110156044
2181298997181298998AG34GENICpossibly homozygous110156045
2181299127181299128AG3GENIChomozygous110156046
2181299134181299135GA6GENIChomozygous110156047
2181299219181299220CT27GENICpossibly homozygous110156048
2181299345181299346TC25GENIChomozygous110156049
2181299375181299376TG17GENIChomozygous110156050
2181299550181299551AG57GENICheterozygous110156051
2181299593181299594AC30GENIChomozygous110156052