chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 40699100 40699101 G A 3 GENIC homozygous 803161272 6 40703137 40703138 T C 24 GENIC homozygous 803161273 6 40703561 40703562 G C 16 GENIC homozygous 803161274 6 40704368 40704369 A C 15 GENIC homozygous 803161275 6 40704486 40704487 T G 27 GENIC homozygous 803161276 6 40705871 40705872 T A 30 GENIC homozygous 803161277 6 40706410 40706411 G T 20 GENIC homozygous 803161278 6 40706530 40706531 C T 30 GENIC homozygous 803161279 6 40707165 40707166 C T 12 GENIC homozygous 803161280 6 40707475 40707476 G T 13 GENIC homozygous 803161281 6 40707496 40707497 T G 11 GENIC homozygous 803161282 6 40707995 40707996 G A 11 GENIC homozygous 803161283 6 40708791 40708792 A G 10 GENIC homozygous 803161284 6 40709143 40709144 T A 3 GENIC homozygous 803161285 6 40709153 40709154 T G 5 GENIC homozygous 803161286 6 40709777 40709778 C T 13 GENIC homozygous 803161287 6 40709778 40709779 A G 13 GENIC homozygous 803161288 6 40709853 40709854 T A 3 GENIC homozygous 803161289 6 40709854 40709855 G C 3 GENIC homozygous 803161290 6 40709880 40709881 G A 3 GENIC homozygous 803161291 6 40710413 40710414 T C 16 GENIC possibly homozygous 803161292 6 40712096 40712097 C T 11 GENIC homozygous 803161293 6 40712500 40712501 T A 6 GENIC homozygous 803161294 6 40713315 40713316 T C 17 GENIC homozygous 803161295 6 40713338 40713339 G A 13 GENIC homozygous 803161296