chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7110914052110914053TC46GENIChomozygous138181967
7110914881110914882CG47GENIChomozygous138181968
7110916882110916883CT60GENIChomozygous138181969
7110919218110919219AG46GENIChomozygous138181970
7110919306110919307TA42GENIChomozygous138181971
7110920696110920697GT50GENIChomozygous138181972
7110914375110914376TC26GENIChomozygous154480330
7110914375110914376T26GENICheterozygous403222373
7110918672110918672GGGGGGGTGGGT12GENICpossibly homozygous137974240