chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	50891469	50891470	A	G	31	GENIC	homozygous	48306090
15	50892902	50892903	C	T	24	GENIC	homozygous	48306091
15	50893016	50893017	C	T	29	GENIC	homozygous	48306092
15	50893774	50893775	G	GGTGT	4	GENIC	homozygous	49085901
15	50899227	50899228	T	G	28	GENIC	homozygous	48306095
15	50899283	50899284	T	C	29	GENIC	homozygous	48306096
15	50899486	50899487	A	AGTGTATCCAG	39	GENIC	homozygous	48306097
15	50899828	50899829	T	C	20	GENIC	possibly homozygous	48306098
15	50900395	50900396	A	T	30	GENIC	homozygous	48306099
15	50900536	50900546	TCACTGCGGA	----------	31	GENIC	homozygous	48306100
15	50901086	50901087	C	T	29	GENIC	homozygous	48306101