chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129798708129798709CT18GENIChomozygous982617984
7129799658129799659GA18GENIChomozygous982617985
7129800613129800614CT25GENIChomozygous982617986
7129801117129801118AG13GENIChomozygous982617987
7129801936129801937GA11GENIChomozygous982617988
7129804694129804695TG18GENIChomozygous982617989
7129804776129804777TC17GENIChomozygous982617990
7129804821129804822GA18GENIChomozygous982617991
7129805161129805162TC22GENIChomozygous982617992
7129805282129805283AG18GENIChomozygous982617993
7129805315129805316TC19GENIChomozygous982617994
7129805327129805328GT18GENIChomozygous982617995
7129806000129806001CT28GENIChomozygous982617996
7129806589129806590CT29GENIChomozygous982617997
7129807333129807334GA8GENIChomozygous982617998
7129807636129807637CA6GENIChomozygous982617999
7129808777129808778CT23GENIChomozygous982618000
7129808911129808912GT26GENIChomozygous982618001
7129808987129808988AG28GENIChomozygous982618002
7129810320129810321TC18GENIChomozygous982618003
7129810349129810350TC22GENIChomozygous982618004
7129810795129810796CT28GENIChomozygous982618005
7129810829129810830GA23GENIChomozygous982618006
7129811223129811224AG24GENIChomozygous982618007