chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187453463074534631AG81GENICheterozygous119581454
187453464074534641AG82GENICheterozygous119581455
187456959374569594CG39GENICheterozygous119501602
187459210274592103TC55GENICheterozygous119539634
187459397474593975AG97GENICheterozygous119501616
187459398174593982GA91GENICheterozygous119501617
187462733174627332AG54GENICheterozygous119581456
187465598274655983CA49GENICheterozygous119539638
187468250674682507CT65GENICheterozygous119549281
187468251074682511CT66GENICheterozygous119581457
187468256674682567TC73GENICheterozygous119549282
187472204574722046CG38GENICheterozygous119581458
187473579474735795TC56GENICheterozygous119569401
187473579874735799TC59GENICheterozygous119581459
187478693574786936CG50GENICheterozygous119581460
187479792874797929AG49GENIChomozygous110403897
187491617274916173AT43GENIChomozygous110404131
187492099274920993GA14GENIChomozygous119501672
187492099474920995GA13GENIChomozygous119501673
187492100274921003CA10GENIChomozygous110834534
187492100674921007CA5GENIChomozygous119581461
187492100874921009GA5GENIChomozygous119573185
187492101274921013CA5GENIChomozygous119573186
187493587074935871TC25GENIChomozygous119501677
187493589074935891TA20GENIChomozygous119501678
187493935674939357GT42GENIChomozygous110816149
187493942374939424TA7GENIChomozygous119539659
187493950274939503TC11GENIChomozygous119501680
187493952374939524TG15GENIChomozygous110404199
187493954674939547TC13GENIChomozygous119501681
187493956274939563TG17GENIChomozygous119501682
187493962574939626GA7GENIChomozygous110635700