chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104752589447525895TC27GENIChomozygous116773917
104752653247526533CG32GENIChomozygous116878684
104752857947528580GA21GENIChomozygous116878686
104752930947529310AG34GENIChomozygous116773919
104753041747530418TC15GENIChomozygous116773921
104753094547530946TG5GENIChomozygous117103809
104753315747533158AG24GENIChomozygous116773923
104753357547533576GC31GENIChomozygous116773925
104753505147535052TG11GENIChomozygous116773929
104753589647535897TC24GENIChomozygous116773931
104753640047536401CT18GENIChomozygous116773933
104753690347536904GT30GENIChomozygous116773935
104753695347536954GA16GENIChomozygous116773939
104753695447536955TC17GENIChomozygous116773941
104753722747537228CT17GENIChomozygous116773943
104753730447537305GA12GENIChomozygous116878688
104753748547537486CA17GENIChomozygous116773945
104753898847538989TC19GENIChomozygous116878690
104753900347539004CT24GENIChomozygous116773947
104753938247539383GA23GENIChomozygous116773949
104753990247539903CA19GENIChomozygous116773951
104754037047540371AT34GENIChomozygous116773953
104754094947540950CT30GENIChomozygous116773955
104754239247542393AG27GENIChomozygous116773963
104754251947542520AC25GENIChomozygous116773965
104754329047543291GA27GENIChomozygous116773967
104754336147543362AG16GENIChomozygous116878692
104754411347544114CT31GENIChomozygous116773971
104754545347545454GC24GENIChomozygous116773975
104754637247546373TC33GENIChomozygous116773977
104754638447546385CT34GENIChomozygous116878698