chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195544106955441070AG16GENIChomozygous109736906
195544154055441541CT9GENIChomozygous109736908
195544155655441557CT11GENIChomozygous109736910
195544304455443045GC25GENIChomozygous109736912
195544441855444419AG32GENIChomozygous109736914
195544452655444527TG32GENIChomozygous109736916
195544571955445720AG13GENIChomozygous109736918
195544762855447629AG23GENICpossibly homozygous109736920
195544933555449336GT23GENIChomozygous109736922
195544964955449650AG15GENIChomozygous109736924
195545393755453938GT18GENIChomozygous109736926
195545595055455951CA24GENIChomozygous109789022
195547978755479788CT30GENIChomozygous109736928
195547979055479791GA29GENIChomozygous109736930
195548185055481851TC30GENIChomozygous109736932
195548187655481877GA27GENIChomozygous109736934
195548217355482174CT29GENIChomozygous109736936
195548259855482599CT29GENIChomozygous109736938
195548670355486704GA21GENIChomozygous109736940
195548701155487012AG31GENIChomozygous109736942
195549093555490936TC6GENIChomozygous109736944
195549095255490953TC8GENIChomozygous109736946
195549183455491835CT8GENIChomozygous109736948
195549198355491984GA18GENIChomozygous109736950
195549480955494810CA17GENIChomozygous109736952
195549789655497897AG37GENIChomozygous109736954
195549793855497939GA29GENIChomozygous109736956
195549807155498072TC22GENIChomozygous109736958
195549828555498286GA21GENIChomozygous109736960
195549843855498439CT33GENIChomozygous109736962
195550008855500089CT24GENIChomozygous109736964
195550053755500538TC32GENIChomozygous109736966
195550106455501065CT36GENIChomozygous109736968
195550592855505929TG23GENIChomozygous109736972
195550659755506598AC19GENIChomozygous109736974
195550734655507347GA27GENIChomozygous109736976
195550775455507755TC20GENIChomozygous109736978
195550779155507792CA26GENIChomozygous109736980
195550899955509000AG37GENIChomozygous109736982
195550907455509075CT36GENIChomozygous109736984
195550973155509732GA29GENIChomozygous109736986