chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121011997210119973AC5GENICheterozygous926674915
121017007710170078TC5GENICheterozygous926674916
121017384710173848CT13GENICheterozygous926674917
121017588410175885TC42GENICheterozygous926674918
121018553910185540GA13GENICheterozygous926674919
121018555610185557AG19GENICheterozygous926674920
121018570410185705CT20GENICheterozygous926674921
121018619410186195GA10GENICheterozygous926674922
121018622110186222GA11GENICheterozygous926674923
121018831710188318CT24GENICheterozygous926674924
121018834610188347TC23GENICheterozygous926674925
121018844010188441AG10GENICheterozygous926674926
121018849210188493TC5GENICheterozygous926674927
121018850310188504GA6GENICheterozygous926674928
121018873310188734GA38GENICheterozygous926674929
121018878810188789TC28GENICheterozygous926674930
121018886810188869CT20GENICheterozygous926674931
121018893110188932AG24GENICheterozygous926674932
121018894910188950GA26GENICheterozygous926674933
121018895610188957AG29GENICheterozygous926674934
121018896110188962CT31GENICheterozygous926674935
121018901410189015G-26GENICheterozygous926804929
121018917510189176GT19GENICheterozygous926674936
121018917610189177GC19GENICheterozygous926674937
121018919810189199AT17GENICheterozygous926674938
121018929510189296CT15GENICheterozygous926674939
121018934310189344CA25GENICheterozygous926674940
121018936710189368GA21GENICheterozygous926674941
121018937510189376TC26GENICheterozygous926674942
121018950610189507CT34GENICheterozygous926674943
121018966110189662CT25GENICheterozygous926674944
121019004810190049TC29GENICheterozygous926674945
121019024410190245AG16GENICheterozygous926674946
121019068710190688CT36GENICheterozygous926674947
121019089610190897AG42GENICheterozygous926674948
121019135210191353CT28GENICheterozygous926674949
121019224410192245GA35GENICheterozygous926674950
121019239410192395AG46GENICheterozygous926674951
121019254010192541AG52GENICheterozygous926674952