chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207354669207354677AGTGAGTG--------3GENIChomozygous60158522
2207354835207354836TC17GENIChomozygous59355388
2207355272207355273GA22GENIChomozygous60301194
2207355826207355828TT--7GENICpossibly homozygous59355389
2207355953207355954T-3GENIChomozygous59355390
2207356446207356447GGTT15GENIChomozygous59355392
2207356450207356451TTG15GENICpossibly homozygous59355393
2207356824207356825CCT4GENICheterozygous59355394
2207357065207357066GA20GENIChomozygous59355396
2207357473207357474CT26GENIChomozygous59355397
2207358397207358398AC23GENIChomozygous59355398
2207359740207359741AG17GENICheterozygous59355399
2207360092207360095GTC---3GENIChomozygous59355401
2207360196207360197TC19GENIChomozygous59355402
2207360489207360490GA15GENIChomozygous59355403
2207361253207361254CT25GENIChomozygous59355404
2207361380207361382GG--8GENIChomozygous59771421
2207362199207362200AG28GENIChomozygous59355407