chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107174604571746046TC19GENIChomozygous116630782
107175522771755228TC30GENIChomozygous116630796
107176707671767077CA22GENICpossibly homozygous117131301
107176866471768665TC27GENIChomozygous116630820
107177674971776750AG30GENIChomozygous116630842
107178270871782709GA13GENIChomozygous117131302
107178282271782823AG20GENIChomozygous117131303
107178534971785350TC23GENIChomozygous116630864
107178535071785351AT23GENIChomozygous116630866
107178610371786104TC23GENIChomozygous116630868
107178822171788222CT13GENIChomozygous117104551
107179024271790243TC23GENIChomozygous117131304
107179650171796502GA27GENIChomozygous117131305
107179711571797116GA23GENIChomozygous117131306
107179720671797207GA27GENIChomozygous117131307
107180123871801239GT22GENIChomozygous116630883
107180183171801832AG19GENIChomozygous116630885
107180686971806870AG25GENIChomozygous117083744
107181422671814227CT16GENIChomozygous117131308
107181510171815102AG20GENIChomozygous117083746
107181662871816629GA19GENIChomozygous117131309
107181922971819230GC20GENIChomozygous116630899
107182467971824680GA14GENIChomozygous117131310
107182910471829105AG24GENIChomozygous116630903
107183028371830284GA15GENIChomozygous116630905
107183093071830931TC28GENIChomozygous116630907
107183313271833133AG28GENIChomozygous117131311
107183461671834617GA29GENIChomozygous116630913
107183476371834764GA28GENIChomozygous117131312
107183492071834921GT31GENIChomozygous117131313
107183657371836574TC22GENIChomozygous117083764
107183659271836593TA27GENIChomozygous117131314
107183783771837838GA25GENICpossibly homozygous117131315