chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1839141903914191T22GENICheterozygous140205858
1839565353956536GA21GENIChomozygous140243789
1839639963963997TG21GENIChomozygous140243799
1840389594038960C25GENIChomozygous140205931
1840390314039032C25GENIChomozygous140205932
1840396144039614A15GENIChomozygous140205933
1840398144039814A18GENIChomozygous140205934
1840398384039838C17GENIChomozygous140205935
1840409554040955A19GENIChomozygous140205936
1840409904040991C16GENIChomozygous140205937
1840410694041070C16GENIChomozygous140205938
1840435534043554T13GENIChomozygous140205941
1840458644045865A16GENIChomozygous140205943
1840462354046235A13GENIChomozygous140205945
1840471094047110C11GENIChomozygous140205946
1840475064047506A22GENIChomozygous140205949
1840475874047588G17GENIChomozygous140205950
1840492274049227T18GENIChomozygous140205951
1840547204054721G9GENIChomozygous140205953
1840760154076015A26GENIChomozygous140205955
1840410964041097C24GENIChomozygous141055353
1840330534033054A8GENIChomozygous403427693
1840330534033054AC8GENICheterozygous403427694
1840330534033054AT8GENICheterozygous403427695
1840410964041097CG24GENICheterozygous403427696
1840461624046163A5GENIChomozygous141055354