chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91065857610658577CT20GENIChomozygous117829719
91066751810667519CT20GENIChomozygous117829722
91066756610667567TC17GENIChomozygous117829724
91066792610667927TC17GENIChomozygous117829726
91066869710668698TG15GENIChomozygous117829728
91066996310669964CT22GENIChomozygous117829730
91067206810672069TC19GENIChomozygous117790287
91067746610677467TC18GENIChomozygous117790289
91067822210678223GA30GENICpossibly homozygous117829732
91068334910683350TC15GENIChomozygous117790291
91069233010692331AG26GENIChomozygous117790294
91070897710708978CG16GENIChomozygous117829734
91070963210709633CT7GENIChomozygous120405985
91070967110709672C13GENIChomozygous128679009
91067536710675367T26GENIChomozygous128679005
91070961010709610T3GENIChomozygous128679006
91070963110709632A7GENIChomozygous128679007
91070965110709652A9GENIChomozygous128679008
91068462810684629TC15GENIChomozygous120451913
91070257210702572TAGA22GENIChomozygous133206235
91070658410706584ACACACACACACA2GENIChomozygous133206236
91070876210708768CTGTGG18GENIChomozygous133206237
91070284910702850AG22GENIChomozygous117244404
91070658610706587GA2GENIChomozygous133215972
91070970810709708C22GENIChomozygous128679010
91070971410709715CA24GENIChomozygous117764068
91071113110711132AG20GENIChomozygous117790299
91071197710711977TTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCA11GENIChomozygous128679011
91071661410716615TC8GENIChomozygous117244406
91071661910716620GC8GENIChomozygous117244407
91071662010716621GC8GENIChomozygous117244408
91071672010716722GG18GENIChomozygous128679012
91071767010717670C8GENIChomozygous128679013
91071767210717673AC8GENIChomozygous123119556
91071767510717677GT7GENIChomozygous133206238
91071768810717688T6GENIChomozygous128679014
91071966210719662T17GENIChomozygous128679015
91073254710732549AC15GENIChomozygous133206239
91070971310709714AT24GENIChomozygous117676013
91073156310731564AG26GENIChomozygous117829736