chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 166739132 166739133 T C 26 GENIC homozygous 57770390 3 166739436 166739437 G A 35 GENIC homozygous 57770391 3 166739575 166739576 C A 35 GENIC homozygous 57770392 3 166739771 166739772 C G 30 GENIC homozygous 57770393 3 166740357 166740358 T C 38 GENIC homozygous 57770394 3 166740709 166740710 A G 30 GENIC homozygous 57770395 3 166741254 166741255 C T 25 GENIC homozygous 57770396 3 166741838 166741839 C G 25 GENIC homozygous 57770397 3 166741865 166741866 A G 21 GENIC homozygous 57770398 3 166742009 166742010 A G 10 GENIC homozygous 57770399 3 166742366 166742367 T TTGG 2 GENIC heterozygous 57770401 3 166742474 166742475 A AT 8 GENIC homozygous 57770406 3 166742504 166742505 T C 14 GENIC homozygous 57770408 3 166742720 166742721 A AT 8 GENIC heterozygous 57770409 3 166742720 166742721 A ATT 8 GENIC possibly homozygous 57770410 3 166742740 166742743 TTT --- 10 GENIC homozygous 57770411 3 166742933 166742934 T C 25 GENIC homozygous 57770412 3 166743473 166743474 G A 49 GENIC homozygous 57770413 3 166745488 166745489 T C 30 GENIC homozygous 57770415