chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410427124104272TC26GENIChomozygous998327978
142410436724104368TC27GENIChomozygous998327979
142410441624104417GC28GENIChomozygous998327980
142410456424104565GA27GENIChomozygous998327981
142410471824104719GA39GENIChomozygous998327982
142410474224104743TC39GENIChomozygous998327983
142410961424109615TC22GENIChomozygous998327984
142410964224109643CT25GENIChomozygous998327985
142410982324109824GT36GENIChomozygous998327986
142410989424109895GT24GENIChomozygous998327987
142410999024109991GC38GENIChomozygous998327988
142411653724116538TC22GENIChomozygous998327989
142411671024116711GA25GENIChomozygous998327990
142411704524117046AC39GENIChomozygous998327991
142411943824119439TA40GENIChomozygous998327992
142411988824119889GA29GENIChomozygous998327993
142412123724121238GA23GENIChomozygous998327994
142412148724121488GA31GENIChomozygous998327995
142412186924121870AT20GENIChomozygous998327996
142412329224123293GT25GENICpossibly homozygous998327997
142412331324123314GC21GENIChomozygous998327998
142412389124123892GC24GENIChomozygous998327999
142412462824124629AG20GENIChomozygous998328000
142412524224125243TC28GENIChomozygous998328001