chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 29921565 29921579 TGTGTGTGTGTGTG -------------- 16 GENIC homozygous 50167711 12 29922441 29922443 TT -- 20 GENIC homozygous 50167713 12 29922449 29922451 TT -- 16 GENIC heterozygous 50167715 12 29922466 29922467 T TTG 19 GENIC homozygous 50167717 12 29922532 29922533 C T 46 GENIC homozygous 50167719 12 29924236 29924237 A G 38 GENIC homozygous 50167721 12 29924339 29924340 A G 44 GENIC homozygous 50167723 12 29925303 29925304 C G 45 GENIC homozygous 50167725 12 29925701 29925702 C G 43 GENIC homozygous 50167727 12 29925853 29925854 G A 44 GENIC homozygous 50167729 12 29926237 29926238 A - 23 GENIC homozygous 50167731 12 29926301 29926302 C T 14 GENIC homozygous 50167733 12 29926652 29926653 C - 10 GENIC heterozygous 50167737 12 29927227 29927228 G GTT 36 GENIC homozygous 50167739 12 29927475 29927476 T - 27 GENIC homozygous 50167741 12 29927654 29927655 C T 28 GENIC homozygous 50167743 12 29927794 29927795 A T 25 GENIC homozygous 50167745 12 29929329 29929330 C T 36 GENIC homozygous 50167747 12 29930337 29930338 A G 34 GENIC homozygous 50167749 12 29927237 29927238 A T 35 GENIC homozygous 50540643 12 29927511 29927533 ATATATATATATATATATATAT ---------------------- 9 GENIC homozygous 50540644