chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5101527439101527440GA26GENIChomozygous113941716
5101530646101530647GA51GENICpossibly homozygous113941718
5101531995101531996CT59GENIChomozygous113941720
5101533001101533002GA33GENIChomozygous113941722
5101533949101533950AG6GENIChomozygous113941724
5101534961101534962GA39GENIChomozygous113941726
5101536413101536414AG20GENIChomozygous113941728
5101537721101537722CT28GENIChomozygous113941730
5101540939101540940AC42GENIChomozygous113941732
5101541910101541911TC39GENIChomozygous113941734
5101542929101542930CA38GENIChomozygous113941736
5101544453101544454GA29GENIChomozygous113941738
5101546369101546370TA42GENIChomozygous113941740
5101546370101546371TC42GENIChomozygous113941741
5101551693101551694CT57GENIChomozygous113941743
5101553993101553994GA25GENIChomozygous113941745