chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161058360161058361TC10GENIChomozygous111795890
3161058643161058644CA9GENIChomozygous111795892
3161058647161058648CA9GENIChomozygous111795894
3161059488161059489TC6GENIChomozygous111795898
3161059878161059879TC9GENIChomozygous111795904
3161060166161060167AG7GENIChomozygous111795906
3161060177161060178CG9GENIChomozygous111795908
3161060708161060709GA8GENIChomozygous111795910
3161060829161060830TC6GENIChomozygous111795912
3161061073161061074GA12GENIChomozygous111795914
3161061094161061095CT9GENIChomozygous111795916
3161061238161061239AG6GENIChomozygous111795918
3161061323161061324TC19GENIChomozygous111795920
3161061385161061386TG15GENIChomozygous111795922
3161061582161061583TA7GENIChomozygous111795924
3161061590161061591GA7GENIChomozygous111795926
3161061895161061896TA12GENIChomozygous111795928
3161062696161062697AT9GENIChomozygous111795930
3161062940161062941TC5GENIChomozygous111795932
3161063349161063350TC9GENIChomozygous111795934
3161063555161063556GA9GENIChomozygous111795936
3161064217161064218AG14GENIChomozygous111795938
3161064660161064661TC13GENIChomozygous111795940
3161064675161064676CT11GENIChomozygous111795942
3161064736161064737TC8GENIChomozygous111795946
3161064738161064739TC7GENIChomozygous111795948
3161064745161064746AG8GENIChomozygous111795950
3161064917161064918GA10GENIChomozygous111795952
3161064961161064962GA6GENIChomozygous111795954
3161065064161065065CT13GENIChomozygous111795958
3161065328161065329AG8GENIChomozygous111795962
3161065348161065349TG9GENIChomozygous111795964
3161065450161065451GA19GENIChomozygous111795966
3161065697161065698AC5GENIChomozygous111795970
3161065737161065738TG7GENIChomozygous111795972
3161065916161065917CT7GENIChomozygous111795974
3161066085161066086AC7GENIChomozygous111795976
3161066141161066142CG6GENIChomozygous111795978
3161066225161066226GA11GENICpossibly homozygous111795980
3161066367161066368AG12GENIChomozygous111795983