chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30912484	30912485	T	C	28	GENIC	homozygous	138953082
11	30913233	30913234	T	G	25	GENIC	homozygous	146237235
11	30919001	30919002	T	C	21	GENIC	homozygous	138953086
11	30921107	30921108	T	C	21	GENIC	homozygous	138953089
11	30921839	30921840	G	A	16	GENIC	homozygous	138953091
11	30923528	30923529	G	A	16	GENIC	homozygous	146237236
11	30924001	30924002	G	A	24	GENIC	homozygous	146237237
11	30925276	30925277	T	G	22	GENIC	homozygous	138953096
11	30925696	30925697	C	T	18	GENIC	homozygous	146237238
11	30927526	30927527	A	C	16	GENIC	homozygous	138953100
11	30927528	30927529	A	G	15	GENIC	homozygous	138953101
11	30917222	30917226	TAAG		17	GENIC	homozygous	146230967
11	30920390	30920392	AA		19	GENIC	homozygous	146230968
11	30929666	30929668	AC		13	GENIC	homozygous	146230969
11	30931281	30931282	C	T	24	GENIC	homozygous	146237239
11	30926349	30926350	T	A	8	GENIC	heterozygous	403302839
11	30926349	30926350	T		8	GENIC	heterozygous	403302838