chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1839319953931996GA17GENIChomozygous148632063
1839565353956536GA11GENIChomozygous140243789
1839639963963997TG27GENIChomozygous140243799
1839993423999343T24GENICheterozygous140205895
1840097674009768A25GENICheterozygous140205902
1840268224026823TC6GENICheterozygous148632064
1840268184026820TC6GENICheterozygous148630196
1840268324026832TC9GENICheterozygous148630197
1840268194026820CG6GENICheterozygous404406381
1840268194026820CT6GENICheterozygous404406382
1840268194026820C6GENICheterozygous404406383
1840389594038960C23GENIChomozygous140205931
1840390314039032C18GENIChomozygous140205932
1840396144039614A20GENIChomozygous140205933
1840398144039814A20GENIChomozygous140205934
1840398384039838C20GENIChomozygous140205935
1840409554040955A24GENIChomozygous140205936
1840409904040991C25GENIChomozygous140205937
1840410694041070C24GENIChomozygous140205938
1840410964041097C21GENIChomozygous141055353
1840410964041097CG21GENICheterozygous403427696
1840435534043554T9GENIChomozygous140205941
1840458644045865A21GENIChomozygous140205943
1840461624046163A17GENICheterozygous141055354
1840462354046235A19GENIChomozygous140205945
1840471094047110C23GENIChomozygous140205946
1840475064047506A31GENIChomozygous140205949
1840475874047588G26GENIChomozygous140205950
1840492274049227T26GENIChomozygous140205951
1840547204054721G22GENIChomozygous140205953
1840760154076015A28GENIChomozygous140205955