chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46213099362130994CT25GENIChomozygous56918013
46213174462131746CA--20GENIChomozygous56918014
46213325462133255AG21GENIChomozygous56918015
46213449462134495AT19GENIChomozygous56918016
46213554462135545AG28GENIChomozygous56918017
46213614862136149AG15GENIChomozygous56918018
46213834662138347A-1GENIChomozygous56918019
46213959362139594TTG6GENIChomozygous56918020
46214307862143079CT18GENIChomozygous56918021
46214571162145712AC14GENIChomozygous56918022
46214892262148923CCCTT13GENIChomozygous56918023
46214912962149130GT19GENIChomozygous56918024
46215645562156456A-2GENICheterozygous56918025
46215793362157934AG18GENIChomozygous56918026
46215797462157975A-9GENICheterozygous56918027
46215876962158770TC18GENIChomozygous56918028
46215986062159861GGGAA19GENIChomozygous56918029
46216279562162796GGCC6GENIChomozygous56918030
46216290562162906CT20GENICpossibly homozygous56918031
46216322262163223TG18GENIChomozygous56918032
46216325662163257A-1GENIChomozygous56918033
46216362062163621TTC27GENIChomozygous56918034
46216390762163908GA29GENIChomozygous56918035
46216428062164281CT28GENIChomozygous56918036