chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 40701109 40701110 G C 27 GENIC homozygous 969780465 6 40702901 40702902 G A 31 GENIC homozygous 969780466 6 40703358 40703359 A G 20 GENIC homozygous 969780467 6 40704005 40704006 T A 26 GENIC possibly homozygous 969780468 6 40704023 40704024 A T 29 GENIC homozygous 969780469 6 40705319 40705320 G T 20 GENIC homozygous 969780470 6 40705433 40705434 G A 25 GENIC homozygous 969780471 6 40705557 40705558 G A 16 GENIC homozygous 969780472 6 40705626 40705627 C T 23 GENIC homozygous 969780473 6 40705673 40705674 A T 32 GENIC homozygous 969780474 6 40705871 40705872 T A 21 GENIC homozygous 969780475 6 40706120 40706121 A G 22 GENIC homozygous 969780476 6 40706121 40706122 A G 22 GENIC homozygous 969780477 6 40707165 40707166 C T 5 GENIC homozygous 969780478 6 40707475 40707476 G T 25 GENIC homozygous 969780479 6 40707496 40707497 T G 27 GENIC homozygous 969780480 6 40708791 40708792 A G 28 GENIC homozygous 969780481 6 40709143 40709144 T A 17 GENIC homozygous 969780482 6 40709153 40709154 T G 19 GENIC homozygous 969780483 6 40709880 40709881 G A 14 GENIC homozygous 969780484 6 40709941 40709942 A G 20 GENIC homozygous 969780485 6 40710134 40710135 G A 20 GENIC homozygous 969780486 6 40713315 40713316 T C 26 GENIC homozygous 969780487 6 40713338 40713339 G A 27 GENIC homozygous 969780488