chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30880472	30880473	T	C	16	GENIC	homozygous	116096109
11	30880650	30880651	A	G	29	GENIC	homozygous	115809846
11	30881286	30881287	T	C	39	GENIC	homozygous	116096111
11	30882026	30882027	G	A	30	GENIC	homozygous	115959985
11	30883071	30883072	A	G	11	GENIC	homozygous	116096113
11	30883155	30883156	T	A	12	GENIC	homozygous	116096115
11	30883216	30883217	T	C	19	GENIC	homozygous	115809852
11	30884111	30884112	A	G	21	GENIC	homozygous	116096119
11	30884206	30884207	T	C	22	GENIC	homozygous	116096121
11	30884486	30884487	A	G	23	GENIC	homozygous	115809854
11	30886612	30886613	G	C	23	GENIC	homozygous	116096123
11	30886629	30886630	A	G	21	GENIC	homozygous	115809860
11	30886858	30886859	A	G	19	GENIC	homozygous	116096125
11	30887179	30887180	T	C	36	GENIC	homozygous	115809862
11	30887639	30887640	T	C	19	GENIC	homozygous	116096127
11	30889474	30889475	T	C	37	GENIC	homozygous	115959988
11	30889480	30889481	A	G	36	GENIC	homozygous	115809866
11	30890808	30890809	A	G	22	GENIC	homozygous	116096131
11	30890862	30890863	G	A	26	GENIC	homozygous	116096133
11	30891923	30891924	T	A	11	GENIC	homozygous	115959989
11	30893243	30893244	G	T	30	GENIC	homozygous	116096135