chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	18535144	18535145	A	G	57	GENIC	homozygous	115276930
12	18535661	18535662	T	C	40	GENIC	homozygous	115276932
12	18536277	18536278	T	G	42	GENIC	homozygous	115276934
12	18537428	18537429	C	T	39	GENIC	homozygous	115276936
12	18537908	18537909	C	T	54	GENIC	homozygous	115276938
12	18538044	18538045	T	C	29	GENIC	homozygous	115276940
12	18538074	18538074		C	29	GENIC	homozygous	128967729
12	18537708	18537709	G	T	37	GENIC	homozygous	115365480
12	18537943	18537944	C		49	GENIC	homozygous	128967725
12	18537953	18537953		C	51	GENIC	homozygous	128967726
12	18538029	18538030	G		33	GENIC	homozygous	128967727
12	18538049	18538051	CA		25	GENIC	possibly homozygous	128967728
12	18538909	18538910	T	C	50	GENIC	homozygous	115276942
12	18539766	18539767	G	C	18	GENIC	heterozygous	130688899
12	18539770	18539771	A	C	17	GENIC	heterozygous	130688900
12	18539775	18539776	G	C	17	GENIC	heterozygous	130688901
12	18540429	18540430	T	C	37	GENIC	homozygous	115276944
12	18542271	18542272	T	C	43	GENIC	homozygous	115276946