chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167085516170855162CT16GENIChomozygous112075984
167085519670855196CTA16GENIChomozygous131180975
167085560470855605CT22GENIChomozygous112075986
167085569970855700GT16GENIChomozygous112075990
167085572170855722TC18GENIChomozygous112075992
167085592570855926TC25GENIChomozygous112075994
167085639770856398AG20GENIChomozygous112075996
167085645570856457GA21GENIChomozygous131180976
167085690170856902AT15GENIChomozygous112075998
167085830270858303GA16GENIChomozygous112076000
167085841370858414TC23GENIChomozygous112076002
167085849270858493TC23GENIChomozygous112076004
167085849970858500TC24GENIChomozygous112076006
167085861770858617TTTT13GENIChomozygous131745776
167085862170858621TTTTTTG11GENIChomozygous131745777
167085873370858733T8GENIChomozygous131180977
167085934370859344TC14GENIChomozygous112076008
167085945770859458AC10GENIChomozygous112132322
167085963970859639C8GENIChomozygous131180978
167085992570859926AT23GENIChomozygous112076010
167086004170860042GA18GENIChomozygous112076012
167086021770860219CA18GENIChomozygous131180979
167086032970860330AG18GENIChomozygous112076014
167086153570861536CT18GENIChomozygous112076016
167086159270861593GA16GENIChomozygous112076018
167086212870862129TG18GENIChomozygous112076020
167086217570862176AG22GENIChomozygous112076022
167086256670862566G16GENIChomozygous131180980
167086264070862641TC14GENIChomozygous112076024
167086390770863908CT19GENIChomozygous112076026
167086413570864136TC14GENIChomozygous112076028
167086578470865785GA21GENIChomozygous112076030
167086810170868102TC23GENIChomozygous112076032
167086812270868123GA25GENIChomozygous112076034
167086812970868130TC25GENIChomozygous112076036
167086847870868479CT21GENIChomozygous112076038
167086877970868780CG18GENIChomozygous112076040