chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144970459144970460GA61GENIChomozygous118516023
7144970757144970758CT50GENIChomozygous118516024
7144970779144970780TC52GENIChomozygous115946228
7144971875144971876TC62GENIChomozygous115946234
7144972795144972796TC58GENIChomozygous115946238
7144973167144973168TC51GENIChomozygous115946242
7144973423144973424TC72GENIChomozygous115946246
7144974283144974284TA52GENIChomozygous118516025
7144975358144975358TGT52GENIChomozygous135187469
7144973628144973629A12GENIChomozygous135187467
7144973860144973860T48GENIChomozygous135187468
7144974291144974291TTG52GENIChomozygous128532279
7144976899144976900AG65GENIChomozygous115946270
7144977697144977698CT57GENIChomozygous118516026
7144979963144979965AC46GENIChomozygous135187470
7144980645144980646GA75GENICpossibly homozygous118516027
7144982309144982310AG49GENIChomozygous115946305
7144982692144982693CT62GENICpossibly homozygous115946307
7144983245144983246GA65GENIChomozygous115946309
7144983615144983616GA49GENIChomozygous115946311
7144983660144983660T34GENICpossibly homozygous128532283
7144984384144984385GT62GENIChomozygous115946313
7144984677144984677ACACACGCGCGCGTGTACATGCGCGCGTGTGGGTACACAC35GENIChomozygous128532284
7144984960144984960ACACACAG19GENICheterozygous135187471
7144984968144984968AC27GENICheterozygous128532285
7144985188144985189CT45GENIChomozygous118516029
7144986918144986924TATGTG27GENIChomozygous135187472
7144986995144986997AT42GENIChomozygous135187473
7144987703144987704AG47GENIChomozygous115946331
7144989799144989800G63GENIChomozygous135187474
7144991494144991495GA67GENIChomozygous118516030
7144983456144983457GA24GENICheterozygous131882914