chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122161612421616125GGC42GENICheterozygous50112071
122161622021616221AAT30GENICheterozygous50507752
122161633121616332AAG40GENICheterozygous50112097
122161633321616334GGT39GENICheterozygous50507754
122161646121616462TTC24GENICheterozygous50112119
122161682021616821G-60GENICheterozygous50112153
122161709821617099GGAT37GENICheterozygous50112181
122161710021617101TTA34GENICheterozygous50112183
122161710521617106T-35GENICheterozygous50112185
122161711121617112AAC37GENICheterozygous50112187
122161793921617941CT--43GENICheterozygous50112250
122161916421619170CACCAT------31GENICheterozygous50537893
122161952621619528AC--41GENICheterozygous50507756
122161952821619529CCTT40GENICheterozygous50507758
122161990221619903CCT7GENICheterozygous50112366
122162050021620501GT36GENIChomozygous50112411
122162065321620654AC12GENICpossibly homozygous50112413
122162081921620820TC17GENICheterozygous50112433
122162111421621115CCA54GENICheterozygous50112449
122162111621621117AAG59GENICheterozygous50112451
122162144221621443G-43GENICheterozygous50112479
122162165121621652TTC37GENICheterozygous50112507
122162225521622256CA3GENIChomozygous50112547
122162241121622412CT6GENIChomozygous50112557
122162245421622455CT10GENIChomozygous50112561
122162274721622748AC21GENICpossibly homozygous50112579
122162281421622815TG17GENICpossibly homozygous50112581
122162286421622865GT18GENIChomozygous50112583
122162314521623149AGGG----4GENICheterozygous50112585
122162339721623398CT24GENICpossibly homozygous50112587
122162346821623469GA18GENICpossibly homozygous50112589
122162352021623521AT12GENIChomozygous50112591
122162368421623685TC6GENICheterozygous50112593
122162377021623771CT21GENICpossibly homozygous50112595
122162383621623837AG18GENICpossibly homozygous50112597
122162384521623846TC15GENICpossibly homozygous50112599
122162408821624089GGTT1GENIChomozygous50537905
122162461721624618TC4GENICheterozygous50112627