chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3108946621108946622TC27GENIChomozygous112348273
3108947626108947627AG27GENIChomozygous111668896
3108947627108947628CG27GENIChomozygous111668897
3108948768108948769CT17GENIChomozygous112348275
3108949312108949313GA30GENIChomozygous112348277
3108951202108951203AG2GENIChomozygous129898298
3108956597108956598AG15GENIChomozygous112348281
3108957745108957746TG20GENICpossibly homozygous111668905
3108960341108960354CGGCAAGGACAAG18GENIChomozygous133474999
3108960505108960506CT17GENIChomozygous112348283
3108960528108960529CT16GENIChomozygous112348285
3108963405108963405T17GENIChomozygous133475000
3108964653108964654TC19GENIChomozygous112348286
3108965650108965651GC16GENIChomozygous112348288
3108969775108969776CT26GENIChomozygous112348290
3108971821108971822TC3GENIChomozygous119721321
3108971822108971823CT3GENIChomozygous119721322
3108971905108971905T20GENIChomozygous127916637
3108971810108971811T2GENIChomozygous127916633
3108971845108971845T9GENIChomozygous127916634
3108971868108971869A14GENIChomozygous127916635
3108971892108971893T18GENIChomozygous127916636
3108971909108971910A20GENIChomozygous127916638
3108971912108971913A20GENIChomozygous127916639
3108971975108971975T13GENIChomozygous127916640
3108971988108971989C12GENIChomozygous127916641
3108971999108972000T8GENIChomozygous127916642
3108972013108972013T6GENIChomozygous127916643
3108972558108972559CT12GENIChomozygous112348292
3108973342108973343C18GENIChomozygous127916658
3108974671108974671C7GENIChomozygous133475001
3108974826108974827CT33GENIChomozygous112348294
3108975685108975686CT15GENIChomozygous111668913
3108976369108976370CT20GENIChomozygous112348296