chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 20,4892258,4892259,A,G,81,GENIC,heterozygous,801143470 20,4892303,4892304,C,T,98,GENIC,heterozygous,801143471 20,4892306,4892307,C,T,99,GENIC,heterozygous,801143472 20,4892832,4892833,G,A,32,GENIC,heterozygous,801143473 20,4892858,4892859,C,T,57,GENIC,heterozygous,801143474 20,4892876,4892877,A,G,76,GENIC,heterozygous,801143475 20,4892878,4892879,T,C,78,GENIC,heterozygous,801143476 20,4892889,4892890,A,G,87,GENIC,heterozygous,801143477 20,4892897,4892898,T,A,92,GENIC,heterozygous,801143478 20,4892902,4892903,G,A,99,GENIC,heterozygous,801143479 20,4892915,4892916,C,T,89,GENIC,homozygous,801143480 20,4892930,4892931,G,C,96,GENIC,heterozygous,801143481 20,4892966,4892967,T,G,149,GENIC,heterozygous,801143482 20,4893007,4893008,A,G,250,GENIC,heterozygous,801143483 20,4893056,4893057,C,T,250,GENIC,heterozygous,801143484 20,4893057,4893058,A,T,248,GENIC,heterozygous,801143485 20,4893058,4893059,T,C,250,GENIC,heterozygous,801143486 20,4893106,4893107,G,A,249,GENIC,heterozygous,801143487 20,4893110,4893111,C,T,249,GENIC,heterozygous,801143488 20,4893162,4893163,A,G,246,GENIC,heterozygous,801143489 20,4893166,4893167,A,G,243,GENIC,heterozygous,801143490 20,4893168,4893169,C,T,242,GENIC,heterozygous,801143491