chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133432071133432072CT32GENIChomozygous56931237
4133433840133433841CT24GENIChomozygous56931238
4133434224133434225AATT13GENIChomozygous56931240
4133434708133434709CT22GENIChomozygous56931241
4133435884133435885TC11GENIChomozygous56931242
4133436441133436442AG28GENICpossibly homozygous56931245
4133436901133436902GT15GENICpossibly homozygous56931246
4133437464133437465CT24GENIChomozygous56931247
4133437478133437479TTACAGATTAACTTACAAACCTG29GENIChomozygous58338194
4133438657133438658TC22GENIChomozygous56931249
4133438684133438685TC29GENIChomozygous56931250
4133440130133440131GGA33GENIChomozygous56931251