chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134760283747602838TC22GENIChomozygous114823543
134760429447604295TC26GENIChomozygous114823545
134760448347604484CT40GENIChomozygous114668699
134760449047604491CT39GENIChomozygous114668701
134760462947604630AC17GENIChomozygous114614998
134760488847604889TC15GENIChomozygous114614999
134760615447606155AT20GENIChomozygous114615002
134760690147606902CT25GENIChomozygous114615003
134760693447606935AG26GENIChomozygous114615005
134760701947607020AG27GENIChomozygous114615006
134760702747607028GA28GENIChomozygous114615007
134760728247607283GT15GENIChomozygous114615008
134760728947607290CT15GENIChomozygous114615009
134760745647607457AG22GENIChomozygous114615010
134760745747607458GA22GENIChomozygous114615011
134760753047607531GA21GENIChomozygous114615012
134760753447607535GT21GENIChomozygous114615013
134760757547607576GA15GENIChomozygous114823547
134760759147607592GC12GENIChomozygous114615014
134760761647607617GA14GENIChomozygous114615015
134760828147608282AG18GENIChomozygous114615017
134760874247608743AG14GENIChomozygous114615018
134760919247609193GA17GENIChomozygous114823549
134761003147610032TG25GENICpossibly homozygous114668741
134761041847610419GA41GENIChomozygous114668743
134761069847610699CA28GENIChomozygous114760246
134761097447610975AG21GENIChomozygous114823551
134761107347611074AG11GENIChomozygous114615019
134761119947611200AT31GENIChomozygous114823553
134761143147611432AG12GENIChomozygous114760248
134761149747611498AG16GENIChomozygous114823555
134761325247613253AG12GENIChomozygous114823557
134761349347613494AC22GENIChomozygous114760256
134761427947614280GA29GENIChomozygous114823559
134761443247614433AG24GENIChomozygous114760258
134761464247614643GA11GENIChomozygous114760260
134761473647614737GA16GENIChomozygous114823561
134761473947614740GA15GENIChomozygous114760262
134761502147615022GA24GENIChomozygous115024845
134761514747615148TC35GENICpossibly homozygous114760264
134761631447616315AT25GENICpossibly homozygous114823563