chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151806951151806952CA17GENIChomozygous118984398
5151807672151807673AG19GENIChomozygous114353407
5151807928151807929AG26GENIChomozygous114542207
5151808196151808197GC33GENICpossibly homozygous118984399
5151808298151808299TC22GENIChomozygous118984400
5151808379151808380AC34GENIChomozygous118984401
5151808512151808513TC23GENIChomozygous119183969
5151808644151808645CT25GENIChomozygous118984402
5151808851151808852CG20GENIChomozygous114542211
5151808997151808998TC25GENICpossibly homozygous114542213
5151809403151809404CT35GENICpossibly homozygous114542215
5151809646151809647GA29GENIChomozygous118984403
5151809715151809716GA31GENICpossibly homozygous118984404
5151810098151810099GT28GENIChomozygous118984405
5151813149151813150GA32GENICpossibly homozygous118984406
5151813513151813514CT27GENICpossibly homozygous118984407