chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249147211249148CA28GENIChomozygous974671904
1211249164211249165AG28GENIChomozygous974671905
1211249514211249515AG24GENIChomozygous974671906
1211249867211249868GA27GENIChomozygous974671907
1211249879211249880GT26GENIChomozygous974671908
1211250193211250194AC19GENIChomozygous974671909
1211250496211250497TC14GENIChomozygous974671910
1211250622211250623CG22GENIChomozygous974671911
1211250623211250624CT22GENIChomozygous974671912
1211250700211250701GA25GENIChomozygous974671913
1211252203211252204AG32GENIChomozygous974671914
1211252677211252678CT12GENIChomozygous974671915
1211254276211254277AC21GENIChomozygous974671916
1211254477211254478TC23GENIChomozygous974671917
1211254496211254497CT27GENIChomozygous974671918
1211255440211255441GT39GENIChomozygous974671919
1211255616211255617AT18GENIChomozygous974671920
1211256722211256723TC39GENIChomozygous974671921
1211257074211257075AG27GENIChomozygous974671922
1211258234211258235GA27GENIChomozygous974671923
1211258541211258542CT19GENIChomozygous974671924
1211258803211258804TC30GENIChomozygous974671925
1211259737211259738AG12GENIChomozygous974671926
1211259868211259869CT26GENIChomozygous974671927
1211260475211260476CG36GENIChomozygous974671928
1211261011211261012GA36GENIChomozygous974671929
1211261278211261279AG34GENIChomozygous974671930
1211261430211261431CT38GENIChomozygous974671931
1211261727211261728CT22GENIChomozygous974671932
1211262253211262254CT23GENIChomozygous974671933
1211262513211262514GA21GENIChomozygous974671934
1211262865211262866AG21GENIChomozygous974671935
1211263517211263518CA27GENIChomozygous974671936
1211264098211264099TG19GENIChomozygous974671937
1211264888211264889CA23GENIChomozygous974671938
1211264889211264890TA23GENIChomozygous974671939