chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46213099362130994CT51GENIChomozygous56918013
46213325462133255AG31GENIChomozygous56918015
46213449462134495AT50GENIChomozygous56918016
46213554462135545AG34GENIChomozygous56918017
46213614862136149AG39GENIChomozygous56918018
46213834662138347A-16GENICpossibly homozygous56918019
46213959362139594TTG16GENIChomozygous56918020
46214307862143079CT27GENIChomozygous56918021
46214571162145712AC28GENIChomozygous56918022
46214892262148923CCCTT47GENIChomozygous56918023
46214912962149130GT21GENIChomozygous56918024
46215793362157934AG19GENIChomozygous56918026
46215797462157975A-7GENIChomozygous56918027
46215814362158149ACACAC------12GENICheterozygous58657564
46215876962158770TC45GENIChomozygous56918028
46215986062159861GGGAA26GENIChomozygous56918029
46216290562162906CT33GENIChomozygous56918031
46216322262163223TG24GENIChomozygous56918032
46216325662163257A-12GENIChomozygous56918033
46216362062163621TTC62GENIChomozygous56918034
46216390762163908GA46GENIChomozygous56918035
46216428062164281CT61GENIChomozygous56918036