chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155143535951435360CG14GENIChomozygous112507241
155143647651436477CT10GENIChomozygous112507243
155143725951437259TATC16GENICpossibly homozygous129255671
155143861051438611AG19GENIChomozygous112507245
155143863551438636A18GENIChomozygous129255672
155143931851439318AAAC11GENIChomozygous129255673
155143993051439931CA4GENIChomozygous118918613
155144053751440538CT20GENIChomozygous112507247
155144086451440865AG7GENIChomozygous118918614
155144117151441172AC3GENIChomozygous129316746
155144117351441174C3GENIChomozygous129255674
155145361251453613GC1GENIChomozygous112809134
155145361451453615GC1GENIChomozygous112809136
155145601451456015CA14GENIChomozygous112507249
155145607051456071GA14GENIChomozygous112507251
155145684451456845GT15GENIChomozygous118918616
155145685651456857TG10GENIChomozygous129316747
155145715951457160T17GENIChomozygous129255675
155145724951457250CT11GENIChomozygous112507253
155145905351459053A17GENIChomozygous129255676
155145957651459577TG16GENIChomozygous112507255
155146034251460343GT15GENIChomozygous112507257
155146108051461081AG17GENIChomozygous112507259
155146122451461225GA20GENIChomozygous112507261
155146125951461260AG22GENIChomozygous112507263
155146196251461963CT17GENIChomozygous112507265
155146200351462025TCAGGATGGAGGGTGACACACT17GENIChomozygous129255677
155146253251462533CG10GENIChomozygous112507267
155146328751463288GA22GENIChomozygous112507269
155146369351463693CCT12GENIChomozygous129255678
155146373751463738AG13GENIChomozygous113070660
155145374651453747GA9GENIChomozygous113054309