chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24750103	24750104	A	AT	19	GENIC	homozygous	50136192
12	24750375	24750376	A	ATG	23	GENIC	homozygous	50136194
12	24750655	24750656	C	CTA	33	GENIC	homozygous	50136196
12	24751790	24751791	C	G	35	GENIC	homozygous	50136198
12	24752328	24752329	A	C	25	GENIC	homozygous	50136200
12	24752337	24752338	A	AC	19	GENIC	homozygous	50136202
12	24752525	24752526	G	GT	18	GENIC	heterozygous	50136206
12	24756036	24756037	A	G	24	GENIC	homozygous	50136214
12	24756442	24756443	C	CT	31	GENIC	homozygous	50136216
12	24756518	24756519	T	TTA	21	GENIC	possibly homozygous	50538676
12	24752525	24752526	G	GTTT	18	GENIC	heterozygous	50508955
12	24752339	24752340	C	A	21	GENIC	homozygous	50538674
12	24754909	24754921	TCCATCCATCCA	------------	21	GENIC	homozygous	50538675
12	24756523	24756524	G	GC	23	GENIC	possibly homozygous	50538677
12	24756527	24756528	A	AC	15	GENIC	heterozygous	50538678
12	24756527	24756528	A	ACCATGTCTCAAAACAATGTGTGTGTGCATGCGTGCGCGCGCGCG	15	GENIC	heterozygous	50538679
12	24759895	24759896	A	G	40	GENIC	homozygous	50136218