chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140756299140756300CA16GENIChomozygous61901740
1140756458140756459AT12GENIChomozygous61901741
1140756502140756503GA13GENIChomozygous61901742
1140756738140756739CG10GENIChomozygous61901743
1140756742140756743TC10GENIChomozygous61901744
1140757180140757181A-17GENIChomozygous60871250
1140757351140757352GA25GENIChomozygous61901745
1140757409140757410GA28GENIChomozygous61901746
1140757487140757488TG17GENIChomozygous61901747
1140757549140757550AT11GENIChomozygous61901748
1140757615140757616TC19GENIChomozygous61901749
1140757729140757730CT24GENIChomozygous61901750
1140757735140757736CT26GENIChomozygous61901751
1140758451140758452TA20GENICpossibly homozygous61901752
1140758794140758795TC19GENIChomozygous61901753
1140758860140758861CCA19GENIChomozygous61901754
1140759215140759216TC14GENIChomozygous61901755
1140759424140759435AGCTTCTGGAG-----------11GENIChomozygous61901756
1140759762140759763CT15GENIChomozygous61901757
1140759973140759974TC14GENIChomozygous60871251
1140759993140759994GT17GENIChomozygous61901758
1140760129140760130AG19GENIChomozygous61901759
1140760294140760295AG7GENIChomozygous60871252
1140760698140760699CT8GENIChomozygous61901760
1140760828140760829GA11GENIChomozygous61901761
1140760919140760920CA10GENIChomozygous61901762
1140760987140760988GC13GENIChomozygous61901763
1140761272140761273TTA12GENIChomozygous61901764
1140761329140761330TC14GENIChomozygous61901765
1140761449140761450GA13GENIChomozygous61901766
1140761482140761483GA14GENIChomozygous61901767
1140761833140761834CA16GENIChomozygous61901768
1140760428140760429GA15GENIChomozygous62160989
1140760430140760431AG15GENIChomozygous62160991