chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144103528144103529TC22GENIChomozygous994184435
7144103747144103748CT9GENIChomozygous994184436
7144105165144105166TG27GENIChomozygous994184437
7144107661144107662AG23GENIChomozygous994184438
7144107952144107953CT24GENIChomozygous994184439
7144109385144109386TC31GENIChomozygous994184440
7144109598144109599CG38GENIChomozygous994184441
7144109629144109630CT32GENIChomozygous994184442
7144109681144109682AC33GENIChomozygous994184443
7144110529144110530CT30GENIChomozygous994184444
7144110901144110902AC30GENIChomozygous994184445
7144111438144111439TC25GENIChomozygous994184446
7144112053144112054GA36GENIChomozygous994184447
7144112570144112571TC35GENIChomozygous994184448
7144115195144115196CT31GENIChomozygous994184449
7144115606144115607AG25GENIChomozygous994184450
7144115720144115721GA26GENIChomozygous994184451
7144115776144115777GA19GENIChomozygous994184452
7144116204144116205GA37GENICpossibly homozygous994184453
7144116838144116839GA33GENIChomozygous994184454
7144116920144116921TC34GENIChomozygous994184455
7144118388144118389AG25GENICpossibly homozygous994184456