chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148731422687314227AG17GENICheterozygous49022696
148731898187318982GA20GENICheterozygous49022719
148734299287342993AG9GENICheterozygous49022841
148734304887343049GA11GENICheterozygous49022843
148734377987343780CT9GENICheterozygous49022858
148734388487343885GA10GENICheterozygous49022860
148735149287351493GA18INTERGENICheterozygous49022880
148735163387351634TC14GENICheterozygous49022882
148735177287351773CT35GENICheterozygous49022886
148735211487352115A-32GENICheterozygous49022888
148735220987352210AG38GENICheterozygous49698089
148735221187352212GA38GENICheterozygous49698091
148735221587352216CG41GENICheterozygous49132604
148735224387352244AAT39GENICheterozygous49022890
148735298787352988GT28GENICheterozygous49022892
148735531887355319AG35GENICheterozygous49022920
148735599987356000TC39GENICheterozygous48814645
148735705987357072TGTATGACATCAC-------------84INTERGENICheterozygous49022933
148735723887357239AAT248INTERGENICheterozygous49022936
148735726987357270CT250INTERGENICheterozygous49733692
148735789087357891CT36INTERGENICheterozygous49022938
148735789187357892AG36INTERGENICheterozygous49022940
148740668587406686TA18GENICheterozygous48814663
148740670787406708CT12GENICheterozygous48814665
148740670987406710AT12GENICheterozygous48814667
148740671187406712GT12GENICheterozygous48814669
148742097787420978CG6GENICheterozygous49023271
148742108287421083GA5GENICheterozygous49023273
148742942487429425TC21GENICheterozygous49023361