chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 52821038 52821039 C T 27 GENIC homozygous 956052029 13 52821186 52821187 G A 25 GENIC homozygous 956052030 13 52821195 52821196 G T 22 GENIC homozygous 956052031 13 52821196 52821197 C T 20 GENIC homozygous 956052032 13 52821228 52821229 A T 25 GENIC homozygous 956052033 13 52821414 52821415 G A 28 GENIC homozygous 956052034 13 52821536 52821537 C T 34 GENIC homozygous 956052035 13 52821852 52821853 G A 36 GENIC homozygous 956052036 13 52822159 52822160 C T 36 GENIC homozygous 956052037 13 52822537 52822538 G A 22 GENIC homozygous 956052038 13 52822641 52822642 T C 23 GENIC homozygous 956052039 13 52822756 52822757 G C 21 GENIC homozygous 956052040 13 52822915 52822916 A G 22 GENIC homozygous 956052041 13 52822922 52822923 G A 27 GENIC homozygous 956052042