chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57351053773510538A10GENIChomozygous128197903
57351264973512650AG22GENIChomozygous113860077
57351361273513613TC21GENIChomozygous113860079
57351393773513938AT19GENIChomozygous113860081
57351522273515226TGAA11GENIChomozygous128197904
57351522973515230AC11GENIChomozygous113860083
57351523373515234AC11GENIChomozygous113860085
57351590573515906A25GENIChomozygous128197905
57351662673516627TC8GENIChomozygous113860087
57351678573516785T13GENICheterozygous131854791
57351931873519319AG26GENIChomozygous113860089
57351995373519954GA12GENIChomozygous113860091
57352037973520380GA6GENIChomozygous113860093
57352215873522159CA19GENIChomozygous113860095
57352328473523285TC27GENIChomozygous113860097
57352351373523514AC10GENIChomozygous113860099
57352649273526493T18GENIChomozygous128197906
57352649873526500AG21GENIChomozygous128197907
57352826873528269GA29GENIChomozygous113860101
57352852573528526CG22GENIChomozygous113860103
57352882873528829AC26GENIChomozygous113860105
57352922173529222TG29GENIChomozygous113860107
57352925573529256TG31GENIChomozygous113860109
57352947873529479CT28GENIChomozygous113860111
57352972173529722GA18GENIChomozygous113860113
57352981173529811AGGAAGG17GENIChomozygous128197908
57352984073529841GA20GENIChomozygous113860115
57352987073529871AG25GENIChomozygous113860121
57352991073529910A28GENIChomozygous128197909
57352993673529937AG27GENIChomozygous113860123
57353033873530339AC16GENIChomozygous113860125
57353065873530659TC36GENIChomozygous113860127
57353131873531319AG36GENIChomozygous113860129
57353184573531848AGC17GENIChomozygous128197910
57353483473534835AG18GENIChomozygous113860131
57353528773535288CT29GENIChomozygous113860133
57354015273540153GT13GENIChomozygous113860135
57354400873544008A27GENICpossibly homozygous128197911
57354676273546763AG8GENIChomozygous113860137
57354880473548804A18GENIChomozygous128197912
57355109973551100AG13GENIChomozygous113860139
57355263273552634AG27GENIChomozygous128197913