chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118936367489363675GT14GENICheterozygous134144670
118936367589363676CG14GENICheterozygous134144671
118937898289378983T26GENIChomozygous128933272
118937899589378995A26GENIChomozygous128933273
118941812289418125CAT25GENIChomozygous128933292
118942966489429665TC11GENICheterozygous134144672
118943010789430108GT4GENICheterozygous134144673
118945567789455693GAGGAGGCAGAGGCAG19GENICheterozygous128933299
118937903489379035AT23GENIChomozygous115998242
118937908889379092CACT17GENICheterozygous130685270
118938732389387324AG45GENIChomozygous116162643
118949165889491659CA63GENICheterozygous118229851
118949166489491665CA66GENICheterozygous118229852
118949187889491879CT29GENICheterozygous133911903
118949190489491905AG28GENICheterozygous133911904
118949203289492033AG20GENICheterozygous134144674
118949239989492400AG8GENICheterozygous131912877
118949657989496580CT13GENICheterozygous133843579
118949662589496626AT15GENICheterozygous133682717
118949673489496735CA24GENICheterozygous130404756
118949682389496824CT14GENICheterozygous133971425
118949697389496974TA30GENICheterozygous118216979
118949702089497021CA40GENICheterozygous128946836
118949713289497133CT25GENICheterozygous134144675
118949714289497143GT23GENICheterozygous134144676