chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67605709076057091AG21GENIChomozygous114862242
67606047076060471TC31GENIChomozygous114862243
67606438176064382GA29GENIChomozygous114862244
67606488576064886TG27GENIChomozygous114862245
67606492976064930GA18GENIChomozygous114862246
67606663376066634CT25GENIChomozygous115258486
67606686376066864CT13GENIChomozygous114862247
67606749776067498AT19GENIChomozygous114862248
67606767876067679CT32GENIChomozygous114862249
67606829176068292TA24GENIChomozygous114862250
67606880876068809AT15GENIChomozygous114862252
67606999176069992CT15GENIChomozygous114862254
67607018376070184AG35GENIChomozygous114862255
67607046876070469AG39GENIChomozygous114862256
67607092576070926CG13GENIChomozygous114862257
67607167076071671CT21GENIChomozygous114862258
67607183276071833GA23GENIChomozygous114862259
67607228276072283AG30GENIChomozygous114862260
67607285376072854GA29GENIChomozygous114862261
67607302176073022GA22GENIChomozygous114862262
67607339476073395GT30GENIChomozygous114862263
67607342476073425CT21GENIChomozygous114862264
67607347576073476TC19GENIChomozygous114862265
67607697076076971TC25GENIChomozygous114862275
67607701076077011GA32GENIChomozygous114862276
67607707976077080GA28GENIChomozygous114862277
67607881176078812AG21GENIChomozygous114862279