chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410380024103801TG7GENIChomozygous976968683
142410385924103860TA19GENIChomozygous976968684
142410427124104272TC30GENIChomozygous976968685
142410436724104368TC34GENIChomozygous976968686
142410441624104417GC29GENIChomozygous976968687
142410456424104565GA27GENIChomozygous976968688
142410471824104719GA32GENIChomozygous976968689
142410474224104743TC39GENIChomozygous976968690
142410961424109615TC25GENIChomozygous976968691
142410964224109643CT26GENIChomozygous976968692
142410982324109824GT24GENIChomozygous976968693
142410989424109895GT17GENIChomozygous976968694
142410999024109991GC14GENIChomozygous976968695
142411609024116091CG8GENIChomozygous976968696
142411653724116538TC29GENIChomozygous976968697
142411671024116711GA42GENIChomozygous976968698
142411704524117046AC32GENIChomozygous976968699
142411943824119439TA21GENIChomozygous976968700
142411988824119889GA31GENIChomozygous976968701
142412028624120287GA22GENIChomozygous976968702
142412123724121238GA25GENIChomozygous976968703
142412148724121488GA41GENIChomozygous976968704
142412186924121870AT34GENIChomozygous976968705
142412329224123293GT27GENIChomozygous976968706
142412331324123314GC31GENIChomozygous976968707
142412389124123892GC39GENIChomozygous976968708
142412462824124629AG19GENIChomozygous976968709
142412524224125243TC34GENIChomozygous976968710