chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 39315304 39315305 T C 7 GENIC homozygous 823642690 12 39315431 39315432 G A 10 GENIC homozygous 823642691 12 39315540 39315544 AACT ---- 9 GENIC homozygous 823642692 12 39315737 39315738 G GTAT 15 GENIC homozygous 823642693 12 39315805 39315806 G A 7 GENIC homozygous 823642694 12 39316196 39316197 T C 14 GENIC homozygous 823642695 12 39316843 39316844 T A 8 GENIC homozygous 823642696 12 39317102 39317103 T C 12 GENIC homozygous 823642697 12 39317409 39317410 A G 8 GENIC homozygous 823642698 12 39317837 39317838 G A 15 GENIC homozygous 823642699 12 39317854 39317855 T C 17 GENIC homozygous 823642700 12 39318268 39318275 TGGTCAC ------- 10 GENIC homozygous 823642701 12 39318571 39318572 T C 11 GENIC homozygous 823642702 12 39318675 39318676 T C 10 GENIC homozygous 823642703 12 39319360 39319361 C T 17 GENIC homozygous 823642704 12 39319527 39319528 C T 17 GENIC homozygous 823642705 12 39319563 39319564 G A 15 GENIC homozygous 823642706 12 39319629 39319630 C T 10 GENIC homozygous 823642707 12 39319835 39319836 A G 7 GENIC homozygous 823642708 12 39320000 39320008 ATGTGCAC -------- 11 GENIC homozygous 823642709 12 39320082 39320083 A C 9 GENIC homozygous 823642710 12 39320394 39320395 G A 14 GENIC homozygous 823642711 12 39321179 39321180 G A 9 GENIC homozygous 823642712 12 39321213 39321214 C T 11 GENIC homozygous 823642713 12 39322648 39322649 C G 8 GENIC homozygous 823642714 12 39322674 39322675 G A 10 GENIC homozygous 823642715 12 39322706 39322707 C T 12 GENIC homozygous 823642716 12 39323091 39323092 G A 9 GENIC homozygous 823642717 12 39323127 39323128 T C 12 GENIC homozygous 823642718 12 39323136 39323137 A G 11 GENIC homozygous 823642719 12 39323213 39323214 T C 12 GENIC homozygous 823642720