chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166031252166031272GCCTTGCGCTCGCTAGGCAA44GENIChomozygous127453278
1166031601166031602CT38GENIChomozygous108355978
1166031632166031633CT45GENIChomozygous108355979
1166031659166031660AG48GENIChomozygous108355980
1166032837166032838TG43GENIChomozygous108355981
1166033099166033099CAT34GENICpossibly homozygous127453279
1166033538166033539CT42GENIChomozygous108355982
1166033544166033545C39GENIChomozygous127453280
1166033956166033957TC55GENIChomozygous108355983
1166034463166034464AG43GENIChomozygous108355984
1166034474166034475GA42GENIChomozygous108355985
1166034506166034507C39GENIChomozygous127453281
1166034841166034842GA47GENIChomozygous108355986
1166035030166035031A25GENIChomozygous127453282
1166035059166035059T19GENIChomozygous127453283
1166036771166036772TC36GENIChomozygous108355987
1166038099166038100TC44GENIChomozygous108355988
1166038102166038103AG45GENIChomozygous108355989
1166038566166038567CT31GENIChomozygous108355990
1166041051166041051GTGTGTGTGA31GENIChomozygous127453284
1166043101166043101CTCT56GENIChomozygous127453285
1166043557166043557CACCCAAA42GENIChomozygous127453286
1166043558166043558GCA38GENIChomozygous127453287
1166044740166044740TT20GENIChomozygous127453288
1166038508166038509CT24GENICpossibly homozygous108751544
1166039394166039395TC47GENIChomozygous108355991
1166040885166040886AG48GENIChomozygous108355992
1166041095166041096AG43GENIChomozygous108355994
1166041868166041869CT59GENIChomozygous108355996
1166043441166043442GA42GENIChomozygous108355997
1166043950166043951AG48GENIChomozygous108355998
1166044972166044973GA42GENIChomozygous108355999