chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107964242107965GGA7GENICheterozygous765902025
1242107979242107980CA12GENIChomozygous664607726
1242108561242108562TC20GENIChomozygous664607727
1242109100242109101GA10GENIChomozygous664607728
1242109190242109191GA17GENIChomozygous664607729
1242109616242109617AG24GENIChomozygous664607730
1242109687242109688CCTT18GENIChomozygous765902027
1242111738242111748CACACACACA----------13GENIChomozygous765902028
1242112448242112449AAC5GENIChomozygous765902032
1242113547242113548CT22GENIChomozygous664607731
1242114398242114399AATC11GENIChomozygous765902033
1242114516242114517GGT11GENICheterozygous765902034
1242114516242114517GGTT11GENICheterozygous765902035
1242115682242115683CA16GENIChomozygous664607732