chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107946242107947GGT19GENIChomozygous750269380
1242107964242107965GGA13GENICpossibly homozygous750269381
1242108561242108562TC22GENIChomozygous638819536
1242109616242109617AG13GENIChomozygous638819537
1242109688242109689T-22GENIChomozygous750269382
1242111737242111738GGCACACACA7GENIChomozygous750269387
1242111893242111894GGA13GENICpossibly homozygous750269388
1242112448242112449AAC11GENIChomozygous750269389
1242112822242112823GA24GENIChomozygous638819538
1242113547242113548CT24GENIChomozygous638819539
1242114398242114399AATC14GENIChomozygous750269390
1242115682242115683CA24GENIChomozygous638819540