chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134760359947603600TA31GENIChomozygous791006067
134760383547603836CT25GENIChomozygous791006068
134760399247603993GA27GENIChomozygous791006069
134760448347604484CT18GENIChomozygous791006070
134760449047604491CT19GENIChomozygous791006071
134760452547604526CT19GENIChomozygous791006072
134760459647604597AG21GENIChomozygous791006073
134760474747604748AG25GENIChomozygous791006074
134760477647604777CA19GENIChomozygous791006075
134760480247604803AC20GENIChomozygous791006076
134760481547604816GA15GENIChomozygous791006077
134760488847604889TC26GENIChomozygous791006078
134760490447604905CT25GENIChomozygous791006079
134760536747605368AC21GENIChomozygous791006080
134760615447606155AT37GENIChomozygous791006081
134760653647606537CT25GENIChomozygous791006082
134760655647606557GA29GENIChomozygous791006083
134760690547606906GA21GENIChomozygous791006084
134760693447606935AG26GENIChomozygous791006085
134760702747607028GA18GENIChomozygous791006086
134760710747607108TC19GENIChomozygous791006087
134760729147607292GA42GENIChomozygous791006088
134760742147607422TC32GENIChomozygous791006089
134760756847607569AG35GENIChomozygous791006090
134760759047607591CT28GENIChomozygous791006091
134760906747609068TC25GENICheterozygous791006092
134760934747609348GA17GENIChomozygous791006093
134760972147609722CT24GENIChomozygous791006094
134761003147610032TG31GENIChomozygous791006095
134761041847610419GA33GENIChomozygous791006096
134761492447614925GC6GENIChomozygous791006097