chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5101527439101527440GA21GENIChomozygous113941716
5101530646101530647GA16GENIChomozygous113941718
5101531995101531996CT24GENIChomozygous113941720
5101533001101533002GA29GENIChomozygous113941722
5101533949101533950AG6GENIChomozygous113941724
5101534961101534962GA32GENIChomozygous113941726
5101536413101536414AG16GENIChomozygous113941728
5101537231101537231T19GENIChomozygous128218252
5101537721101537722CT30GENIChomozygous113941730
5101538630101538630T24GENIChomozygous128218253
5101540003101540011TTAGTCCA19GENIChomozygous128218254
5101540939101540940AC17GENIChomozygous113941732
5101541910101541911TC9GENIChomozygous113941734
5101542569101542573TTAC13GENIChomozygous128218255
5101542929101542930CA27GENIChomozygous113941736
5101544453101544454GA25GENIChomozygous113941738
5101546369101546370TA19GENIChomozygous113941740
5101546370101546371TC19GENIChomozygous113941741
5101551693101551694CT24GENIChomozygous113941743
5101553993101553994GA27GENIChomozygous113941745