chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X117091374117091375GC18GENIChomozygous140688893
X117091659117091659T17GENICpossibly homozygous140594037
X117091716117091717GA21GENIChomozygous140688894
X117092922117092923GA8GENIChomozygous140688895
X117093887117093887AT24GENIChomozygous140594038
X117097487117097488G6GENIChomozygous403487379
X117097499117097500G6GENIChomozygous403487380
X117097499117097500GA6GENICheterozygous403487381
X117097487117097488GA6GENICheterozygous403487378
X117097502117097503G6GENIChomozygous403487382
X117097502117097503GA6GENICheterozygous403487383
X117097950117097951AG22GENIChomozygous140688896
X117098699117098700CT22GENIChomozygous140688897
X117100030117100031CT33GENIChomozygous140688898
X117100253117100254CT19GENIChomozygous140688899
X117103528117103529GT22GENIChomozygous140688900
X117103543117103544CT21GENIChomozygous140688901
X117104047117104048AG17GENIChomozygous140688902
X117104336117104337TC17GENIChomozygous140688903
X117107365117107366GC19GENIChomozygous140688904
X117107480117107481CT18GENIChomozygous140688905