chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50403375	50403376	T	A	8	GENIC	homozygous	50471614
12	50403539	50403540	C	T	12	GENIC	homozygous	50624568
12	50403675	50403676	T	C	9	GENIC	homozygous	50471615
12	50404611	50404612	A	G	7	GENIC	homozygous	50471616
12	50405404	50405405	T	C	1	GENIC	homozygous	50238094
12	50405735	50405736	C	T	6	GENIC	homozygous	50624569
12	50406079	50406080	T	TA	3	GENIC	homozygous	50546905
12	50406607	50406608	G	A	4	GENIC	homozygous	50471618
12	50406758	50406759	C	CTCT	3	GENIC	homozygous	50624570
12	50407352	50407353	C	T	9	GENIC	homozygous	50238102
12	50407353	50407354	T	G	9	GENIC	homozygous	50238104
12	50408372	50408373	A	AC	1	GENIC	homozygous	50624571
12	50408496	50408497	G	GT	5	GENIC	homozygous	50471619
12	50408610	50408611	G	GT	6	GENIC	homozygous	50471620