chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103397342103397347CCCCC16GENIChomozygous128855432
10103409256103409258AC16GENIChomozygous128855433
10103412385103412385TTTC14GENIChomozygous129970914
10103412390103412391T14GENIChomozygous129970915
10103412393103412394T15GENIChomozygous129970916
10103412396103412397T15GENIChomozygous129970917
10103412401103412402CA15GENIChomozygous123417168
10103412404103412405TC15GENIChomozygous123417169
10103412411103412412C13GENIChomozygous129970918
10103412416103412417CT13GENIChomozygous123417171
10103412420103412421TA12GENIChomozygous123417172
10103412422103412423A12GENIChomozygous129970919
10103412425103412426TA11GENIChomozygous123417174
10103412432103412432G13GENIChomozygous129970920
10103412433103412434TG13GENIChomozygous118076315
10103412445103412445GG17GENIChomozygous129970921
10103412453103412453C17GENIChomozygous129970922
10103412473103412473G20GENIChomozygous129970923
10103412475103412476TA20GENIChomozygous116832806
10103412479103412479GGG20GENIChomozygous129970924
10103412481103412482TG22GENIChomozygous116832808
10103412485103412486TA22GENIChomozygous116832809
10103412487103412487C22GENIChomozygous129970925
10103412521103412521C15GENIChomozygous128855434
10103412527103412528C14GENIChomozygous128855435
10103412619103412619T8GENIChomozygous128855436
10103412625103412625G10GENIChomozygous128855437
10103412672103412676TGGC11GENIChomozygous128855438
10103412686103412687CT12GENIChomozygous116713675
10103409047103409048CA19GENIChomozygous116713667
10103409069103409070CA18GENIChomozygous116713669
10103412733103412734C16GENIChomozygous128855439
10103412808103412808G16GENIChomozygous128855440