chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122946080122946081AC25GENIChomozygous115861830
7122946102122946103AC27GENIChomozygous115861832
7122946122122946123AT28GENIChomozygous116082128
7122946123122946124GA28GENIChomozygous116082129
7122946140122946141TA22GENIChomozygous115861834
7122946169122946170AG17GENIChomozygous115861836
7122946243122946245CA16GENIChomozygous128513702
7122946247122946247TT16GENIChomozygous128513703
7122946249122946250GT15GENIChomozygous115861838
7122946250122946251GT15GENIChomozygous122852429
7122946251122946252AT15GENIChomozygous122852430
7122946260122946261C16GENIChomozygous128513704
7122946265122946265T15GENIChomozygous128513705
7122954302122954304CC15GENIChomozygous128513706
7122956000122956011CAGGTCAGACC14GENIChomozygous128513707
7122961491122961492TC16GENICheterozygous129947128
7122961495122961496GT14GENICheterozygous129947129