chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174551469845514699GA28GENICpossibly homozygous47118863
174551475445514755GGC5GENICheterozygous47118864
174551503645515037CCA6GENICheterozygous47118865
174551559645515597AT13GENICheterozygous47118867
174551653645516537CT16GENIChomozygous47118869
174551669745516698TTAGAC3GENIChomozygous47118870
174551848345518484TTG12GENIChomozygous47118873
174551980245519803GC18GENICpossibly homozygous47118874
174552026145520262GA9GENICpossibly homozygous47118875
174552110145521102TC12GENIChomozygous47118885
174552267045522671GA16GENICpossibly homozygous47118886
174552315345523154TTC14GENIChomozygous47118887
174552401045524011GT8GENICheterozygous47118888
174552474545524746TC17GENIChomozygous47118890
174552500945525010AATC15GENIChomozygous47118891
174552508245525083AG20GENICpossibly homozygous47118892
174552526645525267GA18GENIChomozygous47118893
174552589245525893TC10GENICpossibly homozygous47118894
174552661945526620AG19GENIChomozygous47118895
174552669145526692TA7GENIChomozygous47118896
174552752745527528CG7GENIChomozygous47118898
174552757545527576TC6GENICheterozygous47118899
174552792545527926GC20GENIChomozygous47118901
174552809445528098CTAA----10GENICheterozygous47118902
174552816145528162CA13GENIChomozygous47118903
174552817545528176CA10GENIChomozygous47118904
174552868545528686CCTT5GENIChomozygous47118905
174553015245530153G-2GENIChomozygous47118906
174553143545531436G-1GENIChomozygous47118907