chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5101527439101527440GA61GENIChomozygous113941716
5101530646101530647GA59GENIChomozygous113941718
5101531995101531996CT60GENIChomozygous113941720
5101533001101533002GA64GENIChomozygous113941722
5101533949101533950AG22GENIChomozygous113941724
5101534961101534962GA50GENIChomozygous113941726
5101536413101536414AG54GENIChomozygous113941728
5101537721101537722CT52GENIChomozygous113941730
5101538630101538630T48GENIChomozygous128218253
5101537231101537231T46GENICpossibly homozygous128218252
5101540003101540011TTAGTCCA53GENIChomozygous128218254
5101540939101540940AC58GENIChomozygous113941732
5101541910101541911TC61GENIChomozygous113941734
5101542569101542573TTAC64GENIChomozygous128218255
5101542929101542930CA53GENIChomozygous113941736
5101544453101544454GA47GENIChomozygous113941738
5101546369101546370TA45GENIChomozygous113941740
5101546370101546371TC46GENIChomozygous113941741
5101551693101551694CT54GENIChomozygous113941743
5101553993101553994GA52GENIChomozygous113941745