chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83642072636420727GA16GENIChomozygous142062861
83642162736421628CG18GENIChomozygous142062862
83642232136422322GA16GENIChomozygous142062863
83642314936423150AT15GENIChomozygous142062864
83642373336423734TG16GENIChomozygous142062865
83642428136424282GA16GENIChomozygous142062866
83642482136424822TC17GENIChomozygous138307699
83642519936425200GA26GENIChomozygous142062867
83642527536425276TG13GENIChomozygous138307704
83642542936425430GT13GENIChomozygous138307708
83642636736426368AG11GENIChomozygous154496362
83642715836427159GA11GENIChomozygous142062868
83642797436427975TC25GENIChomozygous138307738
83642854236428543AG22GENIChomozygous142062869
83642908636429087CA21GENIChomozygous142062870
83642909436429095AT22GENIChomozygous142062871
83642996436429965TG15GENIChomozygous138307749
83643233636432337TG12GENIChomozygous142062872
83643331136433312AG17GENIChomozygous138307776
83643560236435603GA17GENIChomozygous142062873
83643668736436688GA8GENIChomozygous142062874
83643767536437676GA19GENIChomozygous142062875
83644092536440926AC12GENIChomozygous138307837
83644155336441554AG12GENICheterozygous154495254
83644155336441554A12GENICpossibly homozygous403233905
83642636736426368A11GENICheterozygous403233903
83642636736426368AC11GENICheterozygous403233904
83644155436441555AG12GENICpossibly homozygous142062876
83644155436441555A12GENICheterozygous403233906
83644179136441792AG9GENIChomozygous138307840
83644207236442073CT16GENICheterozygous154495255
83644207236442073C16GENIChomozygous403233907
83644231036442311CA12GENIChomozygous138307847
83644261436442615GA17GENIChomozygous142062877
83644292636442927GA18GENIChomozygous142062878
83644332236443323GA15GENIChomozygous142062879
83642523036425242TTGTTTGTTTGT12GENIChomozygous142022167