chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	3015213	3015214	C	G	38	GENIC	homozygous	115487945
6	3015214	3015215	T	C	38	GENIC	homozygous	115487946
6	3015280	3015281	C	A	31	GENIC	homozygous	114706111
6	3015431	3015432	G	T	18	GENIC	homozygous	118594898
6	3016508	3016509	T	G	31	GENIC	homozygous	114706115
6	3016552	3016553	G	T	27	GENIC	homozygous	114706116
6	3017581	3017582	A	T	20	GENIC	homozygous	114706117
6	3017621	3017622	C	T	25	GENIC	homozygous	118568304
6	3017622	3017623	T	C	25	GENIC	homozygous	118568306
6	3017732	3017733	G	T	17	GENIC	homozygous	114706118
6	3017812	3017813	G	A	32	GENIC	homozygous	114706119
6	3017816	3017817	A	C	33	GENIC	homozygous	118551923
6	3025675	3025676	G	C	21	GENIC	homozygous	114706123
6	3026924	3026925	C	A	28	GENIC	homozygous	118568309
6	3026928	3026929	C	G	28	GENIC	homozygous	118568311
6	3048019	3048020	T	G	14	GENIC	homozygous	114706142
6	3048183	3048184	C	A	10	GENIC	homozygous	115487948
6	3048559	3048560	A	G	14	GENIC	homozygous	114706143
6	3048587	3048588	C	T	18	GENIC	homozygous	114706144
6	3069141	3069142	T	G	37	GENIC	homozygous	115037007
6	3069143	3069144	G	T	36	GENIC	homozygous	118551924
6	3077610	3077611	T	G	24	GENIC	homozygous	115487949
6	3077612	3077613	G	T	23	GENIC	homozygous	118551925
6	3078046	3078047	A	T	31	GENIC	homozygous	114706152