chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1191997993191997994AG64GENIChomozygous108467977
1191998565191998566AG46GENIChomozygous108467978
1192000598192000599TC74GENIChomozygous108467979
1192003006192003007GA56GENIChomozygous108467980
1192003646192003647AG42GENIChomozygous108467981
1192006389192006390CT61GENIChomozygous108467982
1192006822192006823GC61GENIChomozygous108467983
1192007157192007158GA37GENICpossibly homozygous108467984
1192007909192007910GA50GENIChomozygous108467985
1192008064192008065GA40GENICheterozygous108467986
1192009691192009692CT63GENIChomozygous108467987
1192009786192009787TA52GENIChomozygous108467988
1192012228192012229CT39GENIChomozygous108467989
1192012446192012447TC44GENIChomozygous108467990
1192013355192013356TA64GENIChomozygous108467991
1192014375192014376CT61GENIChomozygous108467992
1192014619192014620TC49GENIChomozygous108467993
1192015596192015597CT62GENIChomozygous108467994
1192015927192015928CT70GENIChomozygous108467995
1192016362192016363GA69GENIChomozygous108467996
1192017823192017824TA73GENIChomozygous108467997
1192018268192018269AG59GENIChomozygous108467998
1192019706192019707TG66GENIChomozygous108467999
1192022232192022233CT72GENIChomozygous108468000
1192022479192022480GA73GENIChomozygous108468001