chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121597720915977210GA21GENIChomozygous115420903
121597730215977303GA15GENIChomozygous115420905
121597770815977709GA3GENICheterozygous126220699
121598192515981926CA26GENIChomozygous115420907
121598217515982176TC5GENIChomozygous126167947
121598515415985155GC7GENIChomozygous126220700
121599406215994063CT14GENIChomozygous115420909
121599423415994235GA9GENIChomozygous115420911
121599431515994316AG10GENIChomozygous115420913
121599507315995074AG15GENIChomozygous115420917
121599589115995892GT22GENIChomozygous115269007
121599641515996416CT4GENIChomozygous126220701
121599716615997167CT21GENIChomozygous115420919
121599722615997227AG23GENIChomozygous115420921
121599734215997343TC16GENIChomozygous115420923
121599794415997945GA7GENICheterozygous126220702
121599970915999710CT15GENIChomozygous115420925
121599975915999760CT18GENIChomozygous115420927
121600018216000183AC5GENIChomozygous126220703
121600053416000535TC15GENIChomozygous115420929
121600117316001174TC8GENIChomozygous115420931
121600203316002034AG23GENIChomozygous115420933
121600238116002382GA10GENIChomozygous115420935
121600568316005684CT13GENIChomozygous115420937
121600590716005908TC9GENIChomozygous115420939
121600768616007687AC18GENIChomozygous115420941
121600879516008796AG15GENIChomozygous115420943
121600901716009018TC14GENIChomozygous115420945
121600924616009247AG13GENIChomozygous115420947
121600963716009638CT11GENIChomozygous115420949
121601035116010352AC16GENIChomozygous115269009
121601044516010446CT19GENIChomozygous115269011
121601053216010533CT11GENIChomozygous115420951
121601066516010666TC29GENIChomozygous115269013
121601117816011179GA15GENIChomozygous115420953