chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2236987409236987410CT22GENIChomozygous111030063
2236987633236987634TG14GENIChomozygous110321880
2236988361236988362GA26GENIChomozygous111030065
2236988400236988401GA24GENIChomozygous111030067
2236988536236988537AG12GENIChomozygous111030069
2236988884236988885CT14GENIChomozygous111030071
2236988929236988930CT16GENIChomozygous111030073
2236989313236989314CT22GENIChomozygous111030075
2236989331236989332TC25GENIChomozygous111030077
2236989432236989433TC18GENIChomozygous111030079
2236989600236989601AC14GENIChomozygous111030081
2236990010236990011GA16GENIChomozygous111030083
2236990032236990033CT14GENIChomozygous111030085
2236990036236990037TC12GENIChomozygous111030086
2236990271236990272TC15GENIChomozygous111030088
2236990890236990891TC20GENIChomozygous111030090
2236991124236991125AG14GENIChomozygous111030092
2236991381236991382TG17GENIChomozygous110321884
2236991625236991626AC22GENIChomozygous111030094
2236991668236991669AC20GENIChomozygous111030096
2236991758236991759TA20GENIChomozygous111030098
2236991815236991816CT27GENIChomozygous111030100
2236991829236991830CG26GENIChomozygous111030102
2236992330236992331AG25GENIChomozygous111030104
2236992407236992408GC26GENIChomozygous111030106
2236992422236992423CT30GENIChomozygous111030108
2236992828236992829GA19GENIChomozygous111030110
2236992840236992841TC16GENIChomozygous111030112
2236992969236992970TA14GENIChomozygous111030114
2236993058236993059TA15GENIChomozygous111030116
2236993240236993241GA14GENIChomozygous110321894
2236993370236993371AG23GENIChomozygous111030118
2236993930236993931TC18GENIChomozygous111030120
2236993945236993946TA20GENIChomozygous110321895
2236994397236994398TC14GENIChomozygous110321899
2236994660236994661CT24GENIChomozygous111030122
2236995142236995143AG28GENIChomozygous111030124
2236995182236995183GA26GENIChomozygous111030126
2236995367236995368GA23GENIChomozygous111030128
2236995442236995443AG21GENIChomozygous110321901
2236995743236995744TC20GENIChomozygous111030130