chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	176698442	176698443	T	C	28	GENIC	homozygous	111842261
3	176698562	176698563	T	G	16	GENIC	homozygous	111842263
3	176699234	176699235	G	A	17	GENIC	homozygous	111842265
3	176699604	176699605	G	A	15	GENIC	homozygous	112219096
3	176699931	176699932	C	T	14	GENIC	homozygous	111842267
3	176700144	176700145	T	C	14	GENIC	homozygous	111842269
3	176700799	176700800	A	G	31	GENIC	homozygous	111842283
3	176701155	176701156	C	T	22	GENIC	homozygous	119653213
3	176701443	176701444	G	A	26	GENIC	homozygous	112219098
3	176702150	176702151	C	A	31	GENIC	homozygous	112219099
3	176702168	176702169	C	T	31	GENIC	homozygous	112219100
3	176702401	176702402	A	G	14	GENIC	homozygous	111842295
3	176702634	176702635	G	A	21	GENIC	homozygous	112219101
3	176702731	176702732	A	G	23	GENIC	homozygous	111842297
3	176702961	176702962	A	G	16	GENIC	homozygous	112219102
3	176703040	176703041	A	G	25	GENIC	homozygous	111842301
3	176703386	176703387	A	G	18	GENIC	homozygous	111842303
3	176704603	176704604	T	C	15	GENIC	homozygous	112219103
3	176705665	176705666	C	T	25	GENIC	homozygous	112219104
3	176706207	176706208	T	C	18	GENIC	homozygous	111842320
3	176706247	176706248	A	G	15	GENIC	homozygous	111842322