chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122161612421616125GGC54GENICheterozygous50112071
122161622021616221AAT41GENICheterozygous50507752
122161633121616332AAG50GENICheterozygous50112097
122161633321616334GGT55GENICheterozygous50507754
122161646121616462TTC27GENICheterozygous50112119
122161682021616821G-71GENICheterozygous50112153
122161709821617099GGAT31GENICheterozygous50112181
122161710021617101TTA32GENICheterozygous50112183
122161710521617106T-36GENICheterozygous50112185
122161711121617112AAC38GENICheterozygous50112187
122161793921617941CT--42GENICheterozygous50112250
122161916421619170CACCAT------54GENICheterozygous50537893
122161952621619528AC--46GENICheterozygous50507756
122161990221619903CCT12GENICheterozygous50112366
122162015221620153GGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTATACTCCGTGTGTTGTGTGGGTGGGGTTCACTTTCCTGTGTAGAAGAAGTATA14GENICheterozygous50537894
122162050021620501GT27GENIChomozygous50112411
122162065321620654AC13GENICheterozygous50112413
122162081921620820TC8GENICheterozygous50112433
122162111421621115CCA62GENICheterozygous50112449
122162111621621117AAG68GENICheterozygous50112451
122162165121621652TTC60GENICheterozygous50112507
122162241121622412CT5GENIChomozygous50112557
122162245421622455CT9GENIChomozygous50112561
122162274721622748AC20GENICpossibly homozygous50112579
122162281421622815TG14GENICpossibly homozygous50112581
122162286421622865GT25GENICpossibly homozygous50112583
122162314521623149AGGG----3GENIChomozygous50112585
122162339721623398CT24GENIChomozygous50112587
122162346821623469GA17GENICpossibly homozygous50112589
122162352021623521AT22GENICpossibly homozygous50112591
122162368421623685TC11GENICpossibly homozygous50112593
122162377021623771CT18GENICpossibly homozygous50112595
122162383621623837AG25GENIChomozygous50112597
122162384521623846TC22GENIChomozygous50112599
122162461721624618TC3GENICheterozygous50112627