chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 7,124490607,124490611,CCCT,----,13,GENIC,heterozygous,927228034 7,124490611,124490612,C,G,12,GENIC,heterozygous,927177467 7,124490618,124490619,G,C,9,GENIC,heterozygous,927177468 7,124491014,124491015,C,A,29,GENIC,heterozygous,927177469 7,124491148,124491149,G,-,21,GENIC,heterozygous,927228035 7,124496442,124496443,G,C,19,GENIC,heterozygous,927177470 7,124497378,124497379,C,T,19,GENIC,heterozygous,927177471 7,124503705,124503706,T,A,16,GENIC,heterozygous,927177472 7,124504899,124504900,A,G,7,GENIC,heterozygous,927177473 7,124505978,124505979,G,A,15,GENIC,heterozygous,927177474 7,124538541,124538542,A,AAG,18,GENIC,heterozygous,927228036 7,124538542,124538543,G,T,11,GENIC,heterozygous,927177475 7,124565416,124565417,C,-,29,GENIC,heterozygous,927228037 7,124565428,124565429,G,-,26,GENIC,heterozygous,927228038 7,124565441,124565442,G,C,28,GENIC,heterozygous,927177476 7,124580782,124580783,G,C,31,GENIC,heterozygous,927177477 7,124581195,124581196,G,A,11,GENIC,heterozygous,927177478 7,124597213,124597214,G,A,20,GENIC,heterozygous,927177479 7,124599540,124599542,TT,--,24,GENIC,heterozygous,927228039