chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1173042518173042519G13GENIChomozygous135445597
1173043629173043629C27GENIChomozygous148265094
1173044366173044367TC23GENIChomozygous135748556
1173044430173044431T20GENIChomozygous148265095
1173044581173044581TTAT23GENIChomozygous135445598
1173044737173044738AT18GENIChomozygous135748558
1173044753173044753A14GENIChomozygous135445599
1173044973173044974TC23GENIChomozygous135748559
1173045727173045728AG24GENIChomozygous135748560
1173048232173048233TC20GENIChomozygous135748561
1173048800173048801AC24GENIChomozygous135748562
1173049719173049719AGAG25GENIChomozygous143743043
1173050411173050411T22GENIChomozygous135445600
1173051143173051144TC15GENIChomozygous135748563
1173053191173053192CT16GENIChomozygous135748568
1173054587173054588AG28GENIChomozygous135748572
1173054707173054708TG27GENIChomozygous135748574
1173055572173055573AG9GENIChomozygous135748578
1173057913173057914TA15GENIChomozygous148277645
1173045248173045249CT24GENIChomozygous148277641
1173047656173047657TG23GENIChomozygous148277642
1173051864173051865CT20GENIChomozygous148277643
1173056621173056622CT23GENIChomozygous148277644
1173058252173058253CT9GENIChomozygous148277646
1173059573173059574GT18GENIChomozygous148277648
1173060742173060743C13GENICheterozygous403701428
1173060742173060743CT13GENIChomozygous403701429
1173061146173061147CT11GENIChomozygous135748613
1173062078173062080AG23GENIChomozygous148265096
1173063050173063051GA18GENIChomozygous148277649
1173063414173063415GA19GENIChomozygous148277650
1173063564173063565GA22GENIChomozygous148277651
1173064523173064524AG25GENIChomozygous135748628
1173064538173064539AG23GENIChomozygous135748629
1173066949173066950TC18GENIChomozygous148277652
1173063735173063736GA19GENIChomozygous402973354
1173063732173063733A18GENIChomozygous135445611