chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 13,90809919,90809920,A,T,31,GENIC,homozygous,970741339 13,90811156,90811157,T,A,27,GENIC,homozygous,970741340 13,90811752,90811753,C,T,34,GENIC,homozygous,970741341 13,90814283,90814284,G,A,27,GENIC,homozygous,970741342 13,90814817,90814818,A,G,33,GENIC,homozygous,970741343 13,90816550,90816551,A,G,28,GENIC,homozygous,970741344 13,90817010,90817011,G,A,30,GENIC,homozygous,970741345 13,90817599,90817600,G,A,38,GENIC,homozygous,970741346 13,90818784,90818785,G,A,22,GENIC,homozygous,970741347 13,90818796,90818797,C,T,20,GENIC,homozygous,970741348 13,90819125,90819126,C,T,25,GENIC,homozygous,970741349 13,90821609,90821610,A,T,24,GENIC,homozygous,970741350 13,90821866,90821867,T,C,35,GENIC,homozygous,970741351 13,90822572,90822573,G,A,30,GENIC,homozygous,970741352 13,90823995,90823996,G,C,42,GENIC,homozygous,970741353 13,90824578,90824579,G,T,25,GENIC,homozygous,970741354 13,90824811,90824812,C,T,33,GENIC,homozygous,970741355 13,90825273,90825274,A,G,38,GENIC,homozygous,970741356 13,90825566,90825567,C,T,28,GENIC,homozygous,970741357 13,90826025,90826026,T,C,38,GENIC,homozygous,970741358 13,90827190,90827191,G,A,17,GENIC,homozygous,970741359 13,90827396,90827397,A,G,27,GENIC,homozygous,970741360 13,90827419,90827420,G,A,33,GENIC,homozygous,970741361 13,90829066,90829067,A,G,44,GENIC,homozygous,970741362 13,90830163,90830164,A,G,29,GENIC,homozygous,970741363 13,90830335,90830336,A,G,26,GENIC,homozygous,970741364 13,90830605,90830606,T,C,21,GENIC,homozygous,970741365 13,90830733,90830734,T,C,13,GENIC,heterozygous,970741366