chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103549879835498799TC2GENIChomozygous51407772
103549887635498877C-2GENIChomozygous51407774
103549888535498886AG6GENICheterozygous51407776
103549977535499776CT33GENIChomozygous51407780
103550049235500493GA25GENIChomozygous51407782
103550091135500912CA17GENICheterozygous52137743
103550147635501477CT17GENICpossibly homozygous51407786
103550193435501935TC24GENICpossibly homozygous51407788
103550212335502124AG27GENICpossibly homozygous51407790
103550241935502420AT22GENICpossibly homozygous51407792
103550244035502441GA12GENIChomozygous51407794
103550252435502525CT22GENICheterozygous51407796
103550284635502847GA21GENICpossibly homozygous51407798
103550310435503105A-2GENICheterozygous51846866
103550340235503403GT12GENICpossibly homozygous51407800
103550341135503412GT11GENICpossibly homozygous51407802
103550374535503746A-1GENIChomozygous52137745
103550402135504022TC26GENICpossibly homozygous51407804
103550412735504128AT2GENIChomozygous51407806
103550416035504161AG8GENIChomozygous51407808
103550449635504497AG1GENIChomozygous51407810
103550468835504689GC17GENIChomozygous51407812
103550511535505116TC13GENIChomozygous51407820
103550536235505363GA16GENIChomozygous51407822
103550590335505904TC19GENIChomozygous51407824