chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 16566562 16566563 C A 24 GENIC homozygous 532348742 10 16566606 16566607 G A 25 GENIC homozygous 532348743 10 16566642 16566643 A G 24 GENIC homozygous 532348744 10 16566899 16566900 A G 25 GENIC homozygous 532348745 10 16567064 16567065 C T 19 GENIC homozygous 532348746 10 16567200 16567201 T C 26 GENIC homozygous 532348747 10 16567562 16567563 G A 10 GENIC homozygous 532348748 10 16567616 16567617 T - 16 GENIC homozygous 694364763 10 16567801 16567802 A G 20 GENIC homozygous 532348749 10 16568112 16568113 T C 44 GENIC possibly homozygous 532348750 10 16568206 16568207 T TA 21 GENIC possibly homozygous 694364764 10 16568283 16568284 C G 23 GENIC homozygous 532348751 10 16568312 16568313 T TA 17 GENIC homozygous 694364765 10 16568571 16568572 T C 22 GENIC homozygous 532348752 10 16568615 16568616 C T 26 GENIC homozygous 532348753 10 16569006 16569007 C G 29 GENIC homozygous 532348754 10 16569322 16569323 C G 21 GENIC homozygous 532348755 10 16569349 16569350 C G 17 GENIC homozygous 532348756 10 16569378 16569379 T C 18 GENIC homozygous 532348757 10 16570475 16570476 C T 20 GENIC homozygous 532348758 10 16571091 16571092 G A 24 GENIC homozygous 532348759 10 16571381 16571382 C T 28 GENIC homozygous 532348760 10 16571571 16571572 C G 22 GENIC homozygous 532348761 10 16573029 16573030 C T 27 GENIC heterozygous 532348762 10 16573574 16573575 A T 34 GENIC homozygous 532348763 10 16574216 16574217 G T 32 GENIC homozygous 532348764 10 16574448 16574449 C T 28 GENIC homozygous 532348765 10 16574755 16574756 G A 19 GENIC homozygous 532348766 10 16575144 16575145 T C 28 GENIC possibly homozygous 532348767 10 16575613 16575614 A C 38 GENIC homozygous 529678404 10 16575873 16575874 A G 15 GENIC heterozygous 529678405 10 16575910 16575911 C T 17 GENIC homozygous 529678406 10 16575973 16575974 G GC 17 GENIC homozygous 694364766 10 16576537 16576538 G GT 9 GENIC possibly homozygous 694364767