chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152533779152533780GA28GENIChomozygous114543694
5152534024152534025CT42GENIChomozygous114354648
5152536560152536561CA29GENIChomozygous114543696
5152537312152537313AG28GENIChomozygous114354660
5152537379152537380AG39GENIChomozygous114354662
5152538762152538763CT40GENIChomozygous114543698
5152540281152540282CT23GENIChomozygous114543700
5152540508152540509AG35GENIChomozygous114354688
5152542029152542030TC27GENICpossibly homozygous114543702
5152543155152543156TC25GENIChomozygous114543704
5152543224152543225TC27GENIChomozygous114543706
5152543318152543319TG33GENIChomozygous114543708
5152543349152543350TC29GENIChomozygous114543710
5152543447152543448TG22GENIChomozygous114543712
5152543484152543485AG21GENIChomozygous114543714
5152543504152543505CT19GENIChomozygous114543716
5152543556152543557CG23GENIChomozygous114543718
5152543595152543596TC20GENIChomozygous114354694
5152543630152543631GA17GENIChomozygous114543720
5152543723152543724AG17GENIChomozygous114354696
5152543798152543799AG19GENIChomozygous114543722
5152544097152544098TC27GENIChomozygous114543724
5152544456152544457GA28GENIChomozygous114543726
5152544820152544821AT7GENIChomozygous114354698
5152545032152545033GA39GENICpossibly homozygous114543728
5152545036152545037TG39GENIChomozygous114543730
5152545312152545313GA35GENIChomozygous114543732
5152545738152545739TC22GENIChomozygous114543734
5152545954152545955GA40GENIChomozygous114543736
5152546926152546927TC35GENIChomozygous114543738
5152547110152547111CT41GENIChomozygous114543740