chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167085516170855162CT47GENIChomozygous112075984
167085519670855196CTA56GENIChomozygous131180975
167085560470855605CT46GENIChomozygous112075986
167085569970855700GT54GENIChomozygous112075990
167085572170855722TC62GENIChomozygous112075992
167085645570856457GA54GENIChomozygous131180976
167085841370858414TC46GENIChomozygous112076002
167085592570855926TC59GENIChomozygous112075994
167085639770856398AG54GENIChomozygous112075996
167085690170856902AT51GENIChomozygous112075998
167085830270858303GA61GENIChomozygous112076000
167085849270858493TC57GENIChomozygous112076004
167085849970858500TC56GENIChomozygous112076006
167085861770858617TTTT38GENIChomozygous131745776
167085862170858621TTTTTTG25GENICpossibly homozygous131745777
167085873370858733T63GENIChomozygous131180977
167085934370859344TC71GENIChomozygous112076008
167085963970859639C59GENIChomozygous131180978
167085992570859926AT51GENIChomozygous112076010
167086004170860042GA40GENIChomozygous112076012
167086021770860219CA44GENIChomozygous131180979
167086032970860330AG75GENIChomozygous112076014
167086153570861536CT53GENIChomozygous112076016
167086159270861593GA46GENICpossibly homozygous112076018
167086212870862129TG47GENIChomozygous112076020
167086217570862176AG53GENIChomozygous112076022
167086256670862566G39GENICpossibly homozygous131180980
167086264070862641TC44GENIChomozygous112076024
167086390770863908CT52GENIChomozygous112076026
167086413570864136TC44GENIChomozygous112076028
167086578470865785GA69GENIChomozygous112076030
167086810170868102TC53GENIChomozygous112076032
167086812270868123GA55GENIChomozygous112076034
167086812970868130TC54GENIChomozygous112076036
167086847870868479CT46GENIChomozygous112076038
167086877970868780CG48GENIChomozygous112076040
167085945770859458AC53GENIChomozygous112132322
167086159470861595GA49GENICheterozygous112358548