chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181167576411675765AG20GENIChomozygous140262054
181167760511677605A9GENIChomozygous140209468
181167798211677983TC15GENIChomozygous140262055
181167818011678181CT14GENIChomozygous140262056
181167889011678891AG20GENIChomozygous140262057
181167890811678909CA22GENIChomozygous140262058
181168180311681806AGC19GENIChomozygous140209469
181168232911682329C10GENIChomozygous140209470
181168371611683717AG24GENIChomozygous140262059
181168949611689498AC7GENICpossibly homozygous140209472
181168987611689876T17GENIChomozygous140209473
181169091811690919TC20GENIChomozygous140262060
181169233011692331CT19GENIChomozygous140262061
181169233211692333TC19GENIChomozygous140262062
181168232311682324GC10GENICheterozygous403780359
181168232511682326G10GENIChomozygous403947337
181168232511682326GC10GENICheterozygous403947338
181168232311682324G10GENIChomozygous403780358
181168232711682328G10GENICheterozygous404034452
181168232711682328GC10GENIChomozygous404034453
181168592611685927A17GENICheterozygous140926040
181169592611695927CT17GENIChomozygous140262063
181169592711695928CT17GENIChomozygous140262064
181169768711697688AG13GENIChomozygous140262065
181169915611699157GA15GENIChomozygous140262066
181170188611701887T19GENICpossibly homozygous140209474
181170506811705069TC15GENIChomozygous140262067