chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83642072636420727GA46GENIChomozygous142062861
83642162736421628CG39GENIChomozygous142062862
83642232136422322GA39GENIChomozygous142062863
83642277036422771TC13GENIChomozygous138307686
83642314936423150AT43GENIChomozygous142062864
83642373336423734TG27GENIChomozygous142062865
83642428136424282GA40GENIChomozygous142062866
83642482136424822TC35GENIChomozygous138307699
83642519936425200GA37GENIChomozygous142062867
83642527536425276TG47GENIChomozygous138307704
83642542936425430GT31GENIChomozygous138307708
83642636736426368AG28GENIChomozygous154496362
83642715836427159GA51GENIChomozygous142062868
83642797436427975TC44GENIChomozygous138307738
83642854236428543AG40GENIChomozygous142062869
83642908636429087CA50GENIChomozygous142062870
83642909436429095AT50GENIChomozygous142062871
83642996436429965TG44GENIChomozygous138307749
83642636736426368A28GENICheterozygous403233903
83642636736426368AC28GENICheterozygous403233904
83643233636432337TG27GENIChomozygous142062872
83643331136433312AG32GENIChomozygous138307776
83643560236435603GA40GENIChomozygous142062873
83643668736436688GA17GENIChomozygous142062874
83643767536437676GA46GENIChomozygous142062875
83644092536440926AC48GENIChomozygous138307837
83644155336441554AG28GENICheterozygous154495254
83644155336441554A28GENICpossibly homozygous403233905
83644155436441555AG25GENICpossibly homozygous142062876
83644155436441555A28GENICheterozygous403233906
83644179136441792AG29GENIChomozygous138307840
83644207236442073CT36GENICheterozygous154495255
83644207236442073C36GENICpossibly homozygous403233907
83644231036442311CA49GENIChomozygous138307847
83644261436442615GA57GENIChomozygous142062877
83644292636442927GA48GENIChomozygous142062878
83644332236443323GA51GENIChomozygous142062879
83642523036425242TTGTTTGTTTGT37GENIChomozygous142022167