chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55655562756555628AG22GENIChomozygous802923952
55655599956556000CT26GENIChomozygous802923953
55655610056556101TG32GENIChomozygous802923954
55655739456557395TC26GENIChomozygous802923955
55655808156558082AT32GENIChomozygous802923956
55655837556558376TC20GENIChomozygous802923957
55655838456558385CT19GENIChomozygous802923958
55655862056558621GT28GENIChomozygous802923959
55655883856558839AT18GENIChomozygous802923960
55655934256559343TC14GENIChomozygous802923961
55655962256559623GC25GENIChomozygous802923962
55655970656559707CT18GENIChomozygous802923963
55656004456560045CT28GENICheterozygous802923964
55656006956560070GA27GENICheterozygous802923965
55656018356560184GA71GENICheterozygous802923966
55656021256560213CT65GENICheterozygous802923967
55656075356560754TC88GENICheterozygous802923968
55656076056560761TG69GENICheterozygous802923969
55656079556560796CT34GENICheterozygous802923970
55656080256560803CT39GENICheterozygous802923971
55656114056561141GT15GENIChomozygous802923972
55656152156561522AT16GENIChomozygous802923973
55656154356561544GC21GENIChomozygous802923974
55656179556561796GT20GENIChomozygous802923975
55656208056562081CT20GENIChomozygous802923976
55656240856562409AC19GENIChomozygous802923977
55656279956562800GA16GENICpossibly homozygous802923978
55656280856562809AG17GENICpossibly homozygous802923979
55656318756563188TC20GENIChomozygous802923980
55656330756563308TA19GENIChomozygous802923981
55656465956564660CT34GENIChomozygous802923982
55656521156565212AG34GENIChomozygous802923983
55656536856565369AG44GENIChomozygous802923984
55656541656565417GT38GENIChomozygous802923985
55656583756565838CT24GENIChomozygous802923986
55656616956566170TC27GENIChomozygous802923987
55656626256566263CG27GENIChomozygous802923988