chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124771296847712969AT15INTERGENIChomozygous50223115
124771299047712991CA8INTERGENIChomozygous50223117
124771299247712993CA7INTERGENIChomozygous50223119
124771300747713008CA7INTERGENIChomozygous50223121
124771301547713016TA5INTERGENIChomozygous50223125
124771301747713018CA5INTERGENIChomozygous50223127
124771304147713042CA6INTERGENIChomozygous50223133
124771304547713046GA6INTERGENIChomozygous50223135
124771304947713050CA5INTERGENIChomozygous50223137
124771305747713058CA7INTERGENIChomozygous50223139
124771307147713072CA10INTERGENIChomozygous50223141
124771307347713074CA11INTERGENIChomozygous50223143
124771308947713090CA14INTERGENIChomozygous50223145
124771309447713095TC14INTERGENIChomozygous50223147
124771450847714509CCT7INTERGENIChomozygous50223167
124771451147714512A-7INTERGENIChomozygous50223169
124771456747714568GT7INTERGENIChomozygous50223171
124771460847714609CT12INTERGENIChomozygous50223175
124771460947714610AT12INTERGENIChomozygous50223177
124771584747715848TTCA10INTERGENICheterozygous51079936
124771585947715860GGCA12INTERGENICheterozygous51079937
124771587747715878TTCA17INTERGENICheterozygous51079938
124771589847715900CA--21INTERGENICheterozygous50223181
124771591747715918AC20INTERGENICheterozygous51079939
124771591847715919CT19INTERGENICheterozygous50223183
124771592047715921CT19INTERGENICheterozygous51079940
124771592847715929GT18INTERGENICheterozygous50223185
124771594047715941TC16INTERGENICheterozygous51079941
124771595447715955CT8INTERGENICheterozygous50487581
124773541447735417GTT---14INTERGENIChomozygous50223195
124773715847737159CCT11INTERGENIChomozygous50223207
124773716047737161CCA11INTERGENIChomozygous50223209