chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141857864318578644CA10GENIChomozygous113664167
141857894318578944TC22GENIChomozygous113366693
141857918618579187CT20GENIChomozygous113664169
141857949218579493TC23GENIChomozygous113664171
141858532418585324CT17GENIChomozygous129130994
141858632818586329CA14GENIChomozygous113664175
141858902118589022CG19GENIChomozygous113664187
141858784718587848TA25GENIChomozygous113664181
141858847218588473TC25GENIChomozygous113366710
141858863518588636CT19GENIChomozygous113664183
141858868318588684TC26GENIChomozygous113664185
141858037518580376GA12GENIChomozygous113853475
141858307718583078CA11GENIChomozygous113853477
141858475718584758GA17GENIChomozygous113853479
141858664218586643AG22GENIChomozygous113853481
141858721218587213GA22GENIChomozygous113853483
141858059118580592CG8GENIChomozygous118680944
141858594818585949GA26GENICheterozygous118747585
141858595318585953TGTAGTCATGG27GENICheterozygous133022361
141858905318589054CT14GENIChomozygous113664189
141858907018589071TC10GENIChomozygous113664191
141858913918589140CA11GENIChomozygous113664193
141858923318589234TC30GENIChomozygous113366712
141858936218589363CT19GENIChomozygous113664195
141858995818589959AG23GENIChomozygous113664197
141859050818590509GA25GENIChomozygous113664199
141859085018590851CA19GENIChomozygous113664201
141859094618590947CA14GENIChomozygous113853485