chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 11055171 11055172 G A 18 GENIC homozygous 115567901 7 11056124 11056125 C A 26 GENIC homozygous 115567902 7 11056966 11056967 A G 23 GENIC homozygous 115567903 7 11058936 11058937 A T 20 GENIC homozygous 115567907 7 11059847 11059848 G C 24 GENIC homozygous 115567908 7 11060245 11060246 T C 16 GENIC possibly homozygous 115567910 7 11060289 11060290 G A 19 GENIC homozygous 115567911 7 11060290 11060291 C A 19 GENIC homozygous 115567912 7 11060371 11060372 C A 18 GENIC homozygous 115567913 7 11061036 11061037 A G 31 GENIC homozygous 115567914 7 11061072 11061073 G A 29 GENIC homozygous 115567915 7 11061232 11061233 G T 15 GENIC homozygous 115567916 7 11061324 11061325 A G 26 GENIC homozygous 115567917 7 11069186 11069187 C T 30 GENIC homozygous 115567918 7 11071967 11071968 T G 12 GENIC homozygous 115567919 7 11072020 11072021 G T 6 GENIC heterozygous 118391186 7 11072021 11072022 A T 6 GENIC heterozygous 118391187 7 11072022 11072023 A T 6 GENIC heterozygous 118391188 7 11072632 11072633 T G 24 GENIC homozygous 115567924 7 11074261 11074262 A G 24 GENIC homozygous 115567925 7 11074949 11074950 T A 17 GENIC homozygous 115567926 7 11075108 11075109 G A 29 GENIC homozygous 115567927