chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55804397958043980GT27GENIChomozygous113816734
55804449058044491TC18GENIChomozygous113816736
55804561058045611GA9GENIChomozygous113816738
55804607658046077CT31GENIChomozygous113816740
55805117858051179AG36GENIChomozygous113816742
55805208958052090GA22GENIChomozygous113816744
55805225658052257CT25GENIChomozygous113816746
55805309458053095GA16GENIChomozygous113816748
55805582558055826AG7GENIChomozygous113816750
55805690458056905AG29GENIChomozygous113816752
55805746458057465CA31GENICpossibly homozygous113816754
55805951058059511AT30GENIChomozygous113816756
55806015158060152TC31GENICpossibly homozygous113816758
55806540858065409AC32GENIChomozygous113816764
55806671258066713AG11GENIChomozygous118853852
55806689358066894CT5GENIChomozygous119086685
55807171658071717AG23GENIChomozygous113816772
55807235858072359GT33GENIChomozygous113816774
55807339758073398GT18GENIChomozygous113816778
55807364658073647AG36GENIChomozygous113816780
55807495358074954GA19GENIChomozygous113816782
55807569458075695CG28GENIChomozygous113816784
55807617158076172GA36GENIChomozygous113816786
55807619658076197TC28GENIChomozygous113816788
55807652958076530CT29GENIChomozygous113816790
55807658158076582AG26GENIChomozygous113816792
55807340758073408GT18GENIChomozygous118842937