chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99490765494907655GT11GENIChomozygous188753976
99490766294907663TG8GENIChomozygous188753977
99490842694908427CT28GENIChomozygous188753978
99490964694909647AG16GENIChomozygous188753979
99491148894911489GT18GENIChomozygous188753980
99491212594912126CT20GENIChomozygous190678088
99491227394912274TA18GENIChomozygous190678089
99491236794912368AT22GENIChomozygous190678090
99491241694912417CT19GENIChomozygous190678091
99491258394912584CG10GENICpossibly homozygous190678092
99491276694912767GT20GENIChomozygous190678093
99491296894912969AG21GENIChomozygous190678094
99491322994913230CA28GENIChomozygous190678095
99491335994913360CT20GENIChomozygous190678096
99491337094913371AT18GENIChomozygous188753981
99491342694913427AT24GENIChomozygous190678097
99491373494913735AG17GENICpossibly homozygous190678098
99491375494913755CT14GENIChomozygous190678099
99491388794913888AG18GENIChomozygous190678100
99491404594914046GA19GENIChomozygous190678101
99491417494914175TC23GENIChomozygous190678102
99491441394914414TC24GENIChomozygous188753982
99491504794915048TC24GENIChomozygous190678103
99491512394915124AG15GENIChomozygous190678104
99491512494915125TC15GENIChomozygous190678105
99491544894915449GA22GENICpossibly homozygous190678106
99491572194915722CA12GENICpossibly homozygous190678107
99491632294916323AT23GENIChomozygous188753983
99491636294916363AG20GENIChomozygous188753984
99491643194916432AC18GENIChomozygous190678108
99491649094916491TA20GENIChomozygous190678109
99491715594917156GT20GENIChomozygous190678110
99491719294917193TC18GENIChomozygous190678111
99491751494917515CT20GENICpossibly homozygous190678112
99491779994917800TC33GENIChomozygous188753985
99491791094917911GC13GENIChomozygous188753986
99491820094918201AG20GENIChomozygous190678113
99491868294918683CG13GENIChomozygous190678114
99491900994919010GA15GENIChomozygous190678115
99492020194920202AG6GENICheterozygous190678116
99492042094920421TC31GENIChomozygous190678117
99492055994920560CG14GENIChomozygous190678118