chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15769337357693374TC31GENIChomozygous108112106
15769706657697067AG27GENIChomozygous108112107
15769989757699898AG12GENIChomozygous108112108
15769990157699902GA13GENIChomozygous108112109
15770039157700392AG17GENIChomozygous108112110
15770313057703131CG16GENICpossibly homozygous108112111
15770316357703164TA25GENICheterozygous108112112
15770730457707305TG21GENICpossibly homozygous108112113
15770745957707460AC20GENIChomozygous108112114
15770891057708911GT31GENIChomozygous108112115
15771262657712627CT22GENIChomozygous108857538
15771332657713327TG29GENIChomozygous108112116
15771818457718185AG26GENIChomozygous108112119
15771909657719097TC24GENIChomozygous108112120
15772261357722614TG16GENIChomozygous108112121
15772548657725487AT15GENIChomozygous108112123
15772549257725493GT17GENICpossibly homozygous108112124
15772592357725924AG31GENIChomozygous108857539
15772831557728316TC34GENIChomozygous108857540
15771070257710703CG26GENIChomozygous108857537
15773041857730419GA23GENIChomozygous108857541
15773151657731517AG23GENIChomozygous108857542
15773284157732842AG27GENIChomozygous108112128
15773353857733539GA22GENIChomozygous108112129
15773759757737598TC22GENIChomozygous108857543
15774065657740657TG27GENIChomozygous108112136
15774134557741346AG15GENICpossibly homozygous108112137
15774659357746594GT17GENICpossibly homozygous108857544
15774682657746827TC21GENIChomozygous108112139
15775114457751145CT13GENIChomozygous108112140
15775428257754283CT19GENIChomozygous108857545
15775520757755208GC29GENIChomozygous108112142
15775637057756371CT26GENIChomozygous108857546