chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3179803390179803391CT9GENIChomozygous58264260
3179803505179803506GA10GENIChomozygous58264262
3179804063179804064AG19GENIChomozygous58264264
3179804075179804076GA21GENIChomozygous58264266
3179804264179804265TC23GENICpossibly homozygous58264268
3179804417179804418TTCACTCA4GENIChomozygous57817875
3179804719179804720TC18GENIChomozygous58264270
3179804759179804760AG30GENICpossibly homozygous58264272
3179805519179805520AG11GENIChomozygous58264274
3179805765179805766TA5GENIChomozygous58264276
3179805808179805809GA16GENICpossibly homozygous58264278
3179806370179806371AG19GENIChomozygous58264280
3179806810179806811GA26GENIChomozygous58264282
3179808187179808188TC12GENICpossibly homozygous58264284
3179808196179808197CA14GENICpossibly homozygous58264286
3179809276179809277TG8GENIChomozygous58264290
3179809611179809612AT22GENIChomozygous58264294
3179810565179810566CCT17GENIChomozygous58264296
3179811691179811693CC--8GENIChomozygous58264298
3179811909179811910TC18GENICpossibly homozygous58264300
3179812247179812248GA15GENIChomozygous58264302
3179812807179812808CT26GENICpossibly homozygous58264304
3179816625179816626CT19GENIChomozygous58264306
3179819949179819950TA13GENICheterozygous58264310
3179820263179820264GA13GENICheterozygous58264312
3179820347179820348AG16GENIChomozygous58264314
3179820486179820487AAAAAC1GENIChomozygous58264315
3179822802179822803TTG21GENIChomozygous58264319
3179823056179823057AC10GENICheterozygous58264321
3179823612179823613A-2GENICheterozygous57817883
3179823848179823855TTGATGT-------2GENIChomozygous58264325
3179824171179824172CCT1GENIChomozygous58264329
3179824244179824245TC11GENICpossibly homozygous58264331
3179825497179825498AC14GENICheterozygous58264333