chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207964192207964193GA29GENIChomozygous611819644
2207968686207968687CCT15GENICpossibly homozygous734888262
2207969018207969020TT--11GENICheterozygous734888263
2207969019207969020T-11GENICheterozygous734888264
2207970104207970105TTGTGC31GENIChomozygous734888265
2207970329207970330T-9GENICheterozygous734888266
2207970759207970760CCAA8GENICheterozygous734888267
2207970759207970760CCAAA8GENICpossibly homozygous734888268
2207973017207973018TC30GENIChomozygous610619825
2207973788207973789AC22GENIChomozygous611819645
2207975285207975286TC33GENIChomozygous611819646
2207976314207976316CA--3GENIChomozygous734888269
2207976323207976333ACGCACGCAC----------9GENICheterozygous734888272
2207977065207977066CT21GENIChomozygous611819647
2207977206207977207GA24GENIChomozygous611819648
2207977546207977547TC12GENIChomozygous611819649
2207977706207977707AG23GENIChomozygous611819650
2207978203207978204T-17GENIChomozygous734888273
2207978261207978262T-15GENICpossibly homozygous734888274
2207979027207979028AG34GENIChomozygous611819651
2207979187207979188AG23GENIChomozygous611819652
2207979227207979228AC34GENIChomozygous611819653
2207979259207979260GA38GENIChomozygous611819654
2207979291207979292CT36GENIChomozygous611819655
2207979456207979457TC30GENIChomozygous611819656
2207979618207979619AG23GENIChomozygous611819657
2207979674207979675TC24GENIChomozygous611819658
2207979864207979865GA17GENIChomozygous611819659
2207980879207980880GT29GENIChomozygous611819660