chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85890960558909606GA23GENIChomozygous53122368
85890990458909905CG27GENIChomozygous52982698
85890997358909974CT25GENIChomozygous52982699
85891001558910016CT30GENIChomozygous52982700
85891081658910817TG29GENIChomozygous53122369
85891100658911007GA19GENIChomozygous53122370
85891138658911387TC29GENIChomozygous52982702
85891148458911485GA12GENIChomozygous52982703
85891149158911492A-9GENIChomozygous53122371
85891187958911880TC5GENIChomozygous52982707
85891193158911932A-7GENIChomozygous52982708
85891201058912011CCTAT1GENIChomozygous52982710
85891221658912217AC17GENIChomozygous52982711
85891302658913027AG20GENIChomozygous53122372
85891302858913029TA20GENIChomozygous53122373
85891323858913239AG18GENIChomozygous52982713
85891412058914121AG22GENIChomozygous52982714
85891427658914277AC19GENIChomozygous53122374
85891526758915268AG11GENIChomozygous52982716
85891555458915555GA27GENIChomozygous52982717
85891573058915731GA21GENIChomozygous53122375
85891620058916201AG25GENICheterozygous53182110
85891646758916468CT48GENIChomozygous52982718
85891751558917523TCCTTCCT--------5GENIChomozygous53122376
85891811958918120T-18GENIChomozygous52982720
85891827558918276CT12GENIChomozygous52982721
85891858858918589AAT11GENIChomozygous53122377
85891942258919423CT30GENIChomozygous53122378
85892596058925961AC18GENIChomozygous53122379
85892905658929057GA24GENIChomozygous53122380
85893149958931500GA23GENIChomozygous52982726
85893212158932122AC28GENIChomozygous52982727
85893270058932701GT25GENIChomozygous52982728
85893282558932829CTCT----17GENIChomozygous52982729
85893285058932866TGTGTGTGTGTGTGTG----------------4GENICheterozygous53122381
85893358358933584AG19GENICheterozygous52661998
85893362758933628GA18GENICheterozygous53122382
85893363158933632GA19GENICheterozygous52982734
85893370758933708TTC17GENIChomozygous53122383
85893411958934120AG22GENIChomozygous53122384
85893577558935776AAT20GENIChomozygous53122385