chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X117091374117091375GC31GENIChomozygous140688893
X117091659117091659T22GENICpossibly homozygous140594037
X117091716117091717GA23GENIChomozygous140688894
X117092922117092923GA11GENIChomozygous140688895
X117093887117093887AT25GENIChomozygous140594038
X117097499117097500G7GENICpossibly homozygous403487380
X117097502117097503GA7GENICheterozygous403487383
X117097487117097488GA5GENIChomozygous403487378
X117097487117097488G5GENICheterozygous403487379
X117097499117097500GA7GENICheterozygous403487381
X117097502117097503G7GENICpossibly homozygous403487382
X117097950117097951AG27GENIChomozygous140688896
X117098699117098700CT29GENIChomozygous140688897
X117100030117100031CT27GENIChomozygous140688898
X117100253117100254CT36GENIChomozygous140688899
X117103528117103529GT30GENIChomozygous140688900
X117103543117103544CT24GENIChomozygous140688901
X117104047117104048AG19GENIChomozygous140688902
X117104336117104337TC29GENIChomozygous140688903
X117107365117107366GC29GENIChomozygous140688904
X117107480117107481CT30GENIChomozygous140688905