chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156522399156522400GGA26GENIChomozygous56668445
5156522551156522552AG26GENIChomozygous56133506
5156524176156524177CCT15GENIChomozygous55932288
5156524646156524647GC25GENIChomozygous55932292
5156525578156525579CCTG37GENIChomozygous55932294
5156526463156526464CT25GENIChomozygous55932296
5156526616156526617AC25GENIChomozygous55932298
5156526957156526958CA12GENIChomozygous55932300
5156527862156527863TG22GENIChomozygous55932304
5156528297156528298AG25GENIChomozygous56826917
5156523695156523704AAAAAAAAA---------8GENICheterozygous56752531
5156523724156523725AT8GENICpossibly homozygous56752533
5156524191156524204TTTTTTTTTTTTC-------------7GENIChomozygous56826911
5156524229156524230GA5GENIChomozygous56826913
5156527991156527992CT36GENIChomozygous56826915
5156529722156529723AC38GENICpossibly homozygous56826919
5156529871156529872AC35GENIChomozygous55932308
5156530304156530305CCCT8GENICpossibly homozygous56495249
5156530307156530308CCTTGCTAGG5GENIChomozygous56495250
5156530314156530315GGCTCTACCACTGAGCTAAA1GENIChomozygous56495251
5156530786156530787GA34GENIChomozygous56826921
5156531013156531014GC32GENIChomozygous55932312
5156531671156531672AG21GENIChomozygous55932314