chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 10,12882631,12882635,ATAT,----,12,GENIC,homozygous,818250434 10,12883170,12883171,C,CA,11,GENIC,homozygous,818250435 10,12883428,12883432,AAAC,----,9,GENIC,homozygous,818250436 10,12885869,12885870,T,C,15,GENIC,homozygous,818250437 10,12886209,12886210,T,G,15,GENIC,homozygous,818250438 10,12886467,12886468,T,C,13,GENIC,homozygous,818250439 10,12886531,12886532,G,A,8,GENIC,homozygous,818250440 10,12886825,12886826,A,G,9,GENIC,homozygous,818250441 10,12887055,12887056,G,A,19,GENIC,homozygous,818250442 10,12887889,12887890,C,A,7,GENIC,homozygous,818250443 10,12888723,12888724,T,A,15,GENIC,homozygous,818250444 10,12889666,12889667,G,C,20,GENIC,homozygous,818250445 10,12889935,12889936,C,G,15,GENIC,homozygous,818250446 10,12889957,12889958,T,C,15,GENIC,homozygous,818250447 10,12890050,12890051,A,G,19,GENIC,homozygous,818250448 10,12890992,12890993,G,A,22,GENIC,homozygous,818250449 10,12891222,12891223,T,C,16,GENIC,homozygous,818250450