chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51690516016905161GA22GENIChomozygous114391993
51690539916905400AT34GENIChomozygous114391995
51690540516905406TC36GENIChomozygous114391997
51690560516905606TC40GENIChomozygous114391999
51690614316906144GA29GENIChomozygous114392001
51690622016906221CT28GENIChomozygous113675389
51690683916906840AT44GENIChomozygous114392003
51690702516907026GC11GENIChomozygous113675391
51690752316907524TC32GENIChomozygous114392009
51690760216907603CT35GENIChomozygous114392011
51690825016908251GA21GENIChomozygous114392021
51690839116908392CT17GENIChomozygous114392023
51690905616909057AG28GENIChomozygous113675399
51691048116910482TC32GENIChomozygous114392025
51691066816910669TC28GENIChomozygous114392027
51691126616911267TC27GENIChomozygous114392029
51691152116911522TC38GENIChomozygous114392031
51691184216911843CT24GENIChomozygous114392033
51691231716912318GA9GENIChomozygous113675403
51691433316914334AG19GENIChomozygous114392035
51691450516914506AG23GENIChomozygous114392037
51691865816918659AT21GENIChomozygous114392048
51691974416919745TC29GENIChomozygous113675415
51692011816920119CT37GENIChomozygous114392052
51692253216922533GT22GENIChomozygous114392054
51692430316924304TC19GENIChomozygous113675423
51692562616925627AG20GENIChomozygous113675427