chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58095030880950309CA15GENIChomozygous55492078
58095118080951181TC12GENIChomozygous55492082
58095150180951502GC19GENIChomozygous55492084
58095260480952605CT18GENIChomozygous55492086
58095271480952715GA14GENIChomozygous55492088
58095365580953656CT12GENIChomozygous55492094
58095402880954029TG14GENIChomozygous55492096
58095423080954235TAAAG-----10GENIChomozygous55492104
58095427080954271TA12GENIChomozygous55492106
58095439580954396AC10GENIChomozygous55492108
58095650680956507TC15GENIChomozygous55492110
58096217580962176AG17GENIChomozygous55492116
58096233980962340AG22GENICheterozygous58069402
58096289180962892CT10GENIChomozygous55492118
58096416280964163TC16GENIChomozygous55492120
58096521580965216TC19GENIChomozygous55492122
58096543380965434CT17GENIChomozygous55492124
58096676280966763CT10GENIChomozygous55492126
58096702380967024CT10GENIChomozygous55492132
58096842880968429AG19GENIChomozygous55492134
58096229380962294TC19GENICheterozygous58135315
58097180480971805TC16GENIChomozygous55492148
58096231480962315GA22GENICheterozygous58135317
58097431080974311TC12GENIChomozygous55492154
58097618180976182CCTA14GENIChomozygous55492156
58097652280976524TG--16GENIChomozygous55492158
58097653780976539TG--16GENIChomozygous55492160
58097969180979695TATC----19GENIChomozygous55492178
58098002580980026GC12GENIChomozygous55492196
58098178380981784AG18GENIChomozygous55492204