chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41620809	41620819	CTCGTCAGCT		51	GENIC	homozygous	133254764
12	41621774	41621775	C	A	62	GENIC	homozygous	115330947
12	41622837	41622837		GT	51	GENIC	homozygous	133254765
12	41623301	41623302	T		18	GENIC	homozygous	133254766
12	41623519	41623519		C	47	GENIC	homozygous	133254767
12	41623532	41623533	T	C	49	GENIC	homozygous	115330951
12	41625119	41625120	C	A	41	GENIC	homozygous	115478119
12	41621531	41621532	C	A	53	GENIC	homozygous	115478107
12	41622677	41622678	C	T	55	GENIC	homozygous	115478109
12	41623210	41623211	G	A	28	GENIC	homozygous	115478111
12	41623223	41623224	C	T	35	GENIC	homozygous	115478113
12	41623470	41623471	T	C	44	GENIC	homozygous	115478115
12	41624862	41624863	A	G	49	GENIC	homozygous	115478117
12	41623312	41623313	T	C	18	GENIC	homozygous	133257840
12	41625830	41625831	G	A	32	GENIC	homozygous	133257841
12	41627007	41627008	C	T	59	GENIC	homozygous	115478121
12	41627195	41627196	A	G	53	GENIC	homozygous	115330956
12	41625886	41625888	TG		26	GENIC	homozygous	133254768