chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107979242107980CA4GENIChomozygous675740516
1242108561242108562TC5GENIChomozygous675740517
1242109100242109101GA6GENIChomozygous675740518
1242109190242109191GA5GENIChomozygous675740519
1242109616242109617AG10GENIChomozygous675740520
1242109687242109688CCTT6GENIChomozygous771578649
1242111738242111748CACACACACA----------1GENIChomozygous771578650
1242112448242112449AAC1GENIChomozygous771578654
1242113547242113548CT6GENIChomozygous675740521
1242114398242114399AATC5GENIChomozygous771578655
1242114516242114517GGT10GENICheterozygous771578656
1242114516242114517GGTT10GENICheterozygous771578657
1242115682242115683CA8GENIChomozygous675740522