chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6108467445108467446CT16GENIChomozygous115472730
6108467652108467653CG16GENIChomozygous115151536
6108467895108467896CT9GENIChomozygous115151537
6108468076108468077CA16GENIChomozygous115472732
6108468386108468387GC17GENIChomozygous115151539
6108468577108468578GA12GENIChomozygous115472734
6108468606108468607CT11GENIChomozygous115151540
6108468761108468762GA7GENIChomozygous115151541
6108468768108468769AG6GENIChomozygous115151543
6108469553108469554AC20GENIChomozygous115151544
6108470605108470606AG8GENIChomozygous115151545
6108471658108471659GT13GENIChomozygous115151548
6108472673108472674CT14GENIChomozygous115472738
6108472992108472993CT6GENIChomozygous115472740
6108473278108473279GC22GENIChomozygous115472742
6108473289108473290TC16GENIChomozygous115151558
6108473569108473570CA5GENIChomozygous115151560
6108473696108473697CT9GENICheterozygous115472744
6108473933108473934CG14GENIChomozygous115151564
6108473949108473950TC12GENIChomozygous115151565
6108474297108474298CT22GENIChomozygous115151567
6108474582108474583CT12GENIChomozygous115151570
6108474594108474595GA9GENIChomozygous115151571
6108475077108475078CT18GENIChomozygous115472746
6108475089108475090TC12GENIChomozygous115151575
6108475106108475107AG16GENIChomozygous115472748
6108475178108475179AG13GENIChomozygous115472750
6108475197108475198CT13GENIChomozygous115472752
6108475440108475441CT15GENIChomozygous115472754
6108475505108475506AG15GENIChomozygous115472756
6108475512108475513AG16GENIChomozygous115472758
6108475653108475654TC20GENIChomozygous115472760
6108475758108475759AG17GENIChomozygous115151577
6108475820108475821AG11GENIChomozygous115472762
6108475944108475945TC8GENIChomozygous115472764
6108475971108475972TC14GENIChomozygous115472766
6108476092108476093CT18GENIChomozygous115472768
6108476132108476133AG7GENIChomozygous115472770
6108476261108476262AG6GENIChomozygous115151580
6108476334108476335CT18GENIChomozygous115472772