chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206276730206276731GC20GENICheterozygous61066527
1206276750206276751GA25GENICpossibly homozygous61066528
1206277019206277021AC--6GENIChomozygous61066529
1206278882206278883A-22GENIChomozygous61066531
1206279112206279113GA27GENIChomozygous61066532
1206279581206279591TTTTGTTTTG----------2GENIChomozygous61066533
1206284363206284364GA34GENIChomozygous61066534
1206284990206284991GA40GENIChomozygous61066535
1206285324206285325GA26GENIChomozygous61066536
1206289468206289469GGGTGT7GENICpossibly homozygous61066538
1206289788206289789C-35GENIChomozygous61066539
1206289979206289980AAT21GENIChomozygous61066540
1206290063206290068ACACA-----21GENICheterozygous61066541
1206290065206290068ACA---21GENIChomozygous61066542
1206290067206290070AAA---17GENICheterozygous61066543
1206290067206290068AAC19GENICpossibly homozygous61066544
1206290069206290070A-17GENICheterozygous61066545
1206290370206290371GGCACA21GENIChomozygous61066546
1206290479206290480GC40GENIChomozygous61066547
1206292200206292201TA15GENICheterozygous61921329
1206292265206292266GGAC12GENICheterozygous61066548
1206292298206292299GA20GENIChomozygous61066549