chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	18535144	18535145	A	G	54	GENIC	homozygous	115276930
12	18535661	18535662	T	C	53	GENIC	homozygous	115276932
12	18536277	18536278	T	G	56	GENIC	homozygous	115276934
12	18537428	18537429	C	T	60	GENIC	homozygous	115276936
12	18537708	18537709	G	T	50	GENIC	homozygous	115365480
12	18537908	18537909	C	T	42	GENIC	homozygous	115276938
12	18537943	18537944	C		38	GENIC	homozygous	128967725
12	18537953	18537953		C	37	GENIC	homozygous	128967726
12	18538029	18538030	G		40	GENIC	homozygous	128967727
12	18538044	18538045	T	C	43	GENIC	homozygous	115276940
12	18538049	18538051	CA		43	GENIC	homozygous	128967728
12	18538074	18538074		C	39	GENIC	homozygous	128967729
12	18538909	18538910	T	C	50	GENIC	homozygous	115276942
12	18539311	18539312	A	C	26	GENIC	heterozygous	134145202
12	18539315	18539316	T	A	23	GENIC	heterozygous	132707851
12	18539322	18539323	G	C	24	GENIC	heterozygous	132707852
12	18539326	18539327	A	C	21	GENIC	heterozygous	133572249
12	18539330	18539333	TGG		22	GENIC	heterozygous	133912129
12	18540429	18540430	T	C	59	GENIC	homozygous	115276944
12	18542271	18542272	T	C	46	GENIC	homozygous	115276946