chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 61634427 61634428 C T 37 GENIC possibly homozygous 806827564 3 61634489 61634490 G A 37 GENIC homozygous 806827565 3 61634527 61634528 C T 37 GENIC homozygous 806827566 3 61638304 61638305 A G 48 GENIC heterozygous 806827567 3 61639427 61639428 C T 50 GENIC homozygous 806827568 3 61641391 61641392 T G 15 GENIC possibly homozygous 806827569 3 61641797 61641798 C T 56 GENIC homozygous 806827570 3 61642548 61642549 C T 48 GENIC homozygous 806827571 3 61642853 61642854 G A 60 GENIC homozygous 806827572 3 61645926 61645927 T G 56 GENIC homozygous 806827573 3 61646262 61646263 A T 43 GENIC possibly homozygous 806827574 3 61646990 61646991 T A 46 GENIC homozygous 806827575 3 61649897 61649898 A G 21 GENIC homozygous 806827576 3 61650345 61650346 T G 54 GENIC homozygous 806827577 3 61650726 61650727 A G 21 GENIC homozygous 806827578