chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1127014000127014001GA22GENIChomozygous62574571
1127017610127017611C-29GENIChomozygous60846576
1127017615127017616C-32GENIChomozygous60846577
1127027836127027837TC42GENICpossibly homozygous60846595
1127028097127028099CA--2GENIChomozygous60846597
1127031248127031250TG--2GENIChomozygous60846602
1127031286127031287TTA6GENICheterozygous62367666
1127032049127032050AAAC32GENIChomozygous60846609
1127032272127032284CACACAGTACGT------------7GENICpossibly homozygous62574572
1127035597127035598AATGCTCG23GENIChomozygous60846632
1127036469127036470AATC37GENIChomozygous60846634
1127059287127059288TTTC20GENICpossibly homozygous60846648
1127062191127062197TGTGTG------40GENICheterozygous62156954
1127062193127062197TGTG----40GENICheterozygous62156956
1127062195127062197TG--40GENICheterozygous62156958
1127063850127063852GT--2GENICheterozygous62156962
1127065448127065449GGAC29GENIChomozygous60846662
1127065539127065541AT--5GENICheterozygous60846664
1127066684127066685CG45GENIChomozygous60846667
1127067566127067567AATG2GENICheterozygous62367674
1127069385127069386A-14GENIChomozygous60846669