chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 76376749 76376750 G C 16 INTERGENIC homozygous 793913156 5 76377021 76377022 A G 13 INTERGENIC homozygous 793913157 5 76392167 76392168 G A 45 GENIC homozygous 793913158 5 76392674 76392675 G A 53 GENIC homozygous 793913159 5 76392872 76392873 G A 47 GENIC homozygous 793913160 5 76394966 76394967 C T 51 GENIC homozygous 793913161 5 76397382 76397383 C G 29 GENIC homozygous 793913162 5 76397531 76397532 G A 39 GENIC homozygous 793913163 5 76401099 76401100 C T 38 GENIC homozygous 793913164 5 76404953 76404954 C T 34 GENIC homozygous 793913165 5 76405391 76405392 C T 29 GENIC homozygous 793913166 5 76412078 76412079 A G 28 GENIC homozygous 793913167 5 76412212 76412213 C T 31 GENIC homozygous 793913168 5 76415705 76415706 C T 43 GENIC homozygous 793913169 5 76415873 76415874 A G 25 GENIC homozygous 793913170 5 76415985 76415986 G T 9 GENIC homozygous 793913171 5 76416301 76416302 C T 25 GENIC homozygous 793913172 5 76416322 76416323 C G 38 GENIC homozygous 793913173 5 76416430 76416431 T A 43 GENIC heterozygous 793913174 5 76416476 76416477 G A 46 GENIC heterozygous 793913175 5 76416524 76416525 A G 32 GENIC heterozygous 793913176 5 76417522 76417523 G T 38 GENIC homozygous 793913177 5 76418810 76418811 C T 39 GENIC heterozygous 793913178