chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1229442461229442462TC30GENIChomozygous61604595
1229442988229442989CCA7GENICheterozygous62556498
1229443005229443006GA11GENICheterozygous61683274
1229443005229443010GAAAG-----12GENICheterozygous62446526
1229443400229443401CT17GENIChomozygous61604596
1229443821229443822CG35GENIChomozygous61604597
1229444829229444830AG31GENIChomozygous61604598
1229445409229445410GC39GENIChomozygous61604599
1229446019229446020AAAG17GENIChomozygous61604600
1229446209229446210GA11GENIChomozygous61604603
1229446255229446268AAAAAAAAAAAAA-------------5GENIChomozygous61604604
1229446519229446520TTGTGTGTGCGTGCGTGCGTGC9GENIChomozygous62556499
1229446540229446541AG12GENIChomozygous61968106
1229447281229447282CT22GENIChomozygous61604605
1229448328229448329AG27GENIChomozygous61604606
1229448989229448990GGCAGAGCGGGATC26GENIChomozygous61108816
1229449925229449926T-20GENICpossibly homozygous61604607
1229449934229449935T-21GENIChomozygous61108817
1229450406229450407CT25GENIChomozygous61108819