chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25485946554859466TG9GENIChomozygous58827735
25486669554866696TC25GENIChomozygous58827742
25486737654867377AG21GENICpossibly homozygous58827743
25486903754869038GGT22GENIChomozygous58827744
25486958854869589TC10GENIChomozygous58827745
25486960254869603TC15GENIChomozygous58827746
25486980954869810AG23GENIChomozygous58827747
25486988054869881GC14GENICpossibly homozygous58827748
25487051554870516AT13GENICpossibly homozygous58827749
25487212854872129GA12GENIChomozygous58827758
25487231154872312GA19GENICpossibly homozygous58827759
25487547954875480AG13GENIChomozygous58827763
25487626354876264GT21GENICpossibly homozygous58827764
25487682454876825AG22GENIChomozygous58827765
25487933954879340TC9GENIChomozygous58827766
25487966454879665GT6GENIChomozygous58827767
25488074754880748AG14GENIChomozygous58827768
25488290754882908A-8GENIChomozygous58827769
25488308254883083TC20GENIChomozygous58827770
25488327454883275TC22GENICpossibly homozygous58827771
25488465654884657TTACAC1GENIChomozygous58827773
25488478454884785TTATAC3GENIChomozygous58827774
25488592054885921CT19GENICpossibly homozygous58827776
25488623654886237CT6GENIChomozygous58827777
25488701154887012GA16GENICpossibly homozygous58827778
25488711854887119CT11GENICpossibly homozygous58827779
25488717254887173TC4GENIChomozygous58827780
25488718754887188CA6GENIChomozygous58827781
25488759154887592CA8GENICpossibly homozygous58827785
25488767254887673CT12GENIChomozygous58827786
25488786554887866GA23GENIChomozygous58827787
25488821454888215CT10GENIChomozygous58827788
25488884254888844TT--9GENICheterozygous58827789
25488987354889874TTA20GENIChomozygous58827790
25489078754890788TG13GENIChomozygous58827793
25489093854890939AAG17GENICpossibly homozygous58827794
25489251154892512TA12GENICheterozygous58827797
25489305754893058TC20GENICpossibly homozygous58827798
25487941454879418AAAT----11GENICheterozygous60668672