chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50403375	50403376	T	A	31	GENIC	homozygous	50471614
12	50403675	50403676	T	C	33	GENIC	possibly homozygous	50471615
12	50404611	50404612	A	G	28	GENIC	homozygous	50471616
12	50404717	50404718	A	T	24	GENIC	homozygous	50471617
12	50405404	50405405	T	C	12	GENIC	homozygous	50238094
12	50406079	50406080	T	TAA	10	GENIC	homozygous	50413541
12	50406185	50406186	C	CT	15	GENIC	possibly homozygous	50238096
12	50406607	50406608	G	A	17	GENIC	homozygous	50471618
12	50406749	50406750	T	TC	3	GENIC	heterozygous	50238098
12	50408496	50408497	G	GT	23	GENIC	homozygous	50471619
12	50408610	50408611	G	GT	18	GENIC	homozygous	50471620