chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	2986982	2986983	G	A	25	GENIC	homozygous	114706096
6	3015280	3015281	C	A	19	GENIC	homozygous	114706111
6	3016366	3016367	G	A	15	GENIC	homozygous	114706112
6	3016383	3016384	G	T	15	GENIC	homozygous	114706113
6	3016401	3016402	G	A	13	GENIC	homozygous	114706114
6	3016508	3016509	T	G	11	GENIC	homozygous	114706115
6	3016552	3016553	G	T	20	GENIC	homozygous	114706116
6	3017581	3017582	A	T	18	GENIC	homozygous	114706117
6	3017732	3017733	G	T	18	GENIC	homozygous	114706118
6	3025675	3025676	G	C	25	GENIC	homozygous	114706123
6	3029204	3029205	A	G	46	GENIC	heterozygous	115036997
6	3029212	3029213	A	T	40	GENIC	heterozygous	115036998
6	3029216	3029217	C	A	41	GENIC	heterozygous	115036999
6	3029225	3029226	A	C	40	GENIC	heterozygous	115037000
6	3040540	3040541	C	T	42	GENIC	heterozygous	114706134
6	3040580	3040581	T	C	44	GENIC	heterozygous	114706135
6	3040590	3040591	C	T	48	GENIC	heterozygous	115233009
6	3043910	3043911	T	C	57	GENIC	heterozygous	115089161
6	3044101	3044102	C	T	8	GENIC	possibly homozygous	114706140
6	3047873	3047874	C	A	18	GENIC	homozygous	114706141
6	3078046	3078047	A	T	21	GENIC	homozygous	114706152
6	3080645	3080646	T	C	16	GENIC	homozygous	114706154
6	3080650	3080651	T	C	13	GENIC	homozygous	114706155