chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	110618558	110618559	A	T	51	GENIC	homozygous	112003879
3	110621031	110621032	C	T	42	GENIC	homozygous	112003881
3	110621910	110621911	A	G	40	GENIC	homozygous	112003883
3	110622819	110622820	C	A	43	GENIC	homozygous	112003885
3	110622982	110622983	A	C	47	GENIC	homozygous	112003887
3	110624496	110624497	G	A	42	GENIC	homozygous	112003889
3	110625631	110625632	T	C	44	GENIC	homozygous	112003891
3	110625834	110625835	T	C	37	GENIC	homozygous	112003893
3	110626881	110626881		ACCTGGT	46	GENIC	homozygous	130907821
3	110627134	110627135	T	C	48	GENIC	homozygous	112003895
3	110627484	110627485	G	A	44	GENIC	homozygous	112003897
3	110628152	110628153	T	C	36	GENIC	homozygous	112003899
3	110631298	110631299	G		46	GENIC	homozygous	127918172
3	110631856	110631857	T	C	53	GENIC	homozygous	111673091
3	110632367	110632368	A	T	55	GENIC	homozygous	111673093
3	110632368	110632369	G	C	54	GENIC	homozygous	111673095
3	110633253	110633254	G	C	51	GENIC	homozygous	111673098
3	110633583	110633583		ACA	35	GENIC	homozygous	127918173
3	110633628	110633629	A	G	42	GENIC	homozygous	111673100
3	110634584	110634585	G	A	39	GENIC	homozygous	111673102
3	110635996	110635997	C	T	54	GENIC	homozygous	112003901
3	110636109	110636110	T	C	50	GENIC	homozygous	111673105
3	110636137	110636138	G	C	48	GENIC	homozygous	111673107
3	110636553	110636554	T	C	38	GENIC	homozygous	111673109
3	110636699	110636700	C	T	47	GENIC	homozygous	111673111
3	110636841	110636842	A	G	35	GENIC	homozygous	111673112
3	110636918	110636919	A	G	33	GENIC	homozygous	111673114