chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151839916118399162TC51GENIChomozygous112464139
151839948818399489GA54GENIChomozygous112464141
151840014618400147GA40GENIChomozygous112464143
151840695818406958A20GENIChomozygous129234591
151840697318406974T22GENIChomozygous129234592
151840697518406976T22GENIChomozygous129234593
151840698118406982AG22GENIChomozygous112999733
151840698618406989GGT22GENIChomozygous129234594
151840700318407004A26GENIChomozygous129234595
151840702618407028AT34GENIChomozygous129234596
151840702918407030T34GENIChomozygous129234597
151840703918407040G37GENIChomozygous129234598
151840704618407047A37GENIChomozygous129234599
151840704918407050GC39GENIChomozygous112999737
151841104318411043TT9GENIChomozygous129234600
151841105918411059C15GENIChomozygous129234601
151841107818411079C19GENIChomozygous129234602
151841108018411081C19GENIChomozygous129234603
151841112218411123C27GENIChomozygous129234604
151841113118411137GGGCCG27GENIChomozygous129234605
151841137818411379C29GENIChomozygous129234606
151841138818411389GA32GENIChomozygous112464145
151841139318411394G32GENIChomozygous129234607
151841139518411396GT32GENIChomozygous112464147
151841140018411401CA34GENIChomozygous112464149
151841141218411413GT36GENIChomozygous112464151
151841143118411432AT42GENIChomozygous112464153
151841143718411437C43GENIChomozygous129234608
151841144218411443A43GENIChomozygous129234609
151841592518415928AAT45GENIChomozygous129234610
151841594118415942C51GENIChomozygous129234611
151841594718415947T53GENIChomozygous129234612