chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144441607644416077GT10GENIChomozygous113742334
144441641344416413T13GENIChomozygous129152856
144441684344416844GA7GENIChomozygous125981815
144441782844417829GA21GENIChomozygous125981817
144441786744417868TC19GENIChomozygous113444658
144441787644417877GA20GENIChomozygous113444660
144441851244418513TA15GENIChomozygous113444662
144442242444422425TA11GENIChomozygous125981821
144442243044422431TC11GENIChomozygous125981823
144442253244422533CT14GENIChomozygous113742346
144442347844423479T6GENICheterozygous134445332
144442508544425086GA6GENIChomozygous125981825
144442698544426986CT18GENIChomozygous125981827
144442769144427691A17GENIChomozygous129152858
144442914944429149G11GENIChomozygous134305073
144442916244429163AG9GENIChomozygous118691614
144442916844429169AG7GENIChomozygous118817338
144442922444429224GACGACGACGAC8GENIChomozygous134445333
144442950744429508T6GENIChomozygous134445334
144442988844429888C12GENICheterozygous134445335
144443027344430274AT1GENIChomozygous132730962
144443567944435680T11GENIChomozygous134445336
144443803144438032TC12GENIChomozygous113742366
144443856744438568GC14GENIChomozygous125981831
144443905144439052TG20GENIChomozygous113742370
144443935244439353T10GENICpossibly homozygous134445337
144444129644441297GA22GENIChomozygous125981833
144444129944441300CT22GENIChomozygous125981835
144444356744443568G23GENIChomozygous134445338
144444366244443663AG13GENIChomozygous125981837
144444366344443664GA13GENIChomozygous125981839
144444394544443946TC11GENIChomozygous113444668
144444511744445118GA10GENIChomozygous125981841
144444858844448589AT5GENIChomozygous134450239
144445217744452178TC17GENIChomozygous125981843
144445771744457718AG16GENIChomozygous113444670
144445975644459757GA11GENIChomozygous125981847
144442060944420610AT13GENIChomozygous113787399