chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101530011715300118GC18GENIChomozygous51624516
101530327815303279CCT27GENIChomozygous51812275
101530459015304591AT27GENIChomozygous51624530
101530571015305711TC24GENIChomozygous51624537
101530576315305764TC25GENIChomozygous51624538
101530603715306038AT16GENIChomozygous51624539
101530606815306069CT15GENIChomozygous51812277
101530609415306095GA21GENIChomozygous51624540
101530617415306175CT31GENIChomozygous51624541
101530657215306573CG21GENIChomozygous51624542
101530683515306836CT26GENIChomozygous51812279
101530696415306965AG17GENIChomozygous51624543
101530731415307315CT28GENIChomozygous51812281
101530755015307551GA24GENIChomozygous51624545