chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	160117220	160117221	G	A	27	GENIC	homozygous	111791348
3	160121364	160121365	T	C	41	GENIC	homozygous	111791350
3	160122035	160122036	A	C	31	GENIC	homozygous	111791352
3	160122802	160122803	T	C	27	GENIC	homozygous	111791354
3	160125087	160125088	T	C	22	GENIC	homozygous	111791356
3	160125187	160125188	C	T	28	GENIC	homozygous	111791358
3	160125308	160125309	T	C	22	GENIC	homozygous	111791360
3	160125819	160125820	G	A	24	GENIC	homozygous	111791366
3	160125987	160125988	A	G	26	GENIC	homozygous	111791368
3	160127632	160127633	T	C	24	GENIC	homozygous	111791370
3	160127970	160127971	A	G	23	GENIC	homozygous	111791372
3	160128055	160128056	G	A	20	GENIC	homozygous	111791374
3	160130184	160130185	A	T	26	GENIC	homozygous	111791376
3	160131879	160131880	T	C	28	GENIC	homozygous	111791378
3	160134869	160134870	C	T	25	GENIC	homozygous	111791386
3	160134924	160134925	G	A	21	GENIC	homozygous	111791388
3	160134959	160134960	G	A	22	GENIC	homozygous	111791390
3	160136723	160136724	C	T	29	GENIC	homozygous	111791394
3	160139923	160139924	T	A	22	GENIC	homozygous	111791396