chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31812086	31812087	T	G	21	GENIC	homozygous	115812554
11	31813099	31813100	C	T	45	GENIC	homozygous	116096985
11	31816607	31816608	C	T	32	GENIC	homozygous	115812558
11	31816630	31816631	T	C	33	GENIC	homozygous	115812560
11	31819202	31819203	G	A	27	GENIC	homozygous	116096988
11	31819852	31819853	C	G	32	GENIC	homozygous	115812568
11	31824572	31824573	A	G	26	GENIC	homozygous	116096990
11	31825714	31825715	A	C	30	GENIC	homozygous	116096992
11	31826107	31826108	T	C	21	GENIC	homozygous	115812572
11	31826979	31826980	G	A	39	GENIC	homozygous	116096994
11	31827086	31827087	T	C	36	GENIC	homozygous	115812578
11	31829285	31829286	A	C	37	GENIC	homozygous	116096996
11	31833603	31833604	T	C	30	GENIC	homozygous	115812586
11	31835049	31835050	A	C	23	GENIC	homozygous	116096998
11	31835709	31835710	T	C	34	GENIC	homozygous	115812590
11	31836429	31836430	T	C	19	GENIC	homozygous	116097000
11	31836441	31836442	G	A	18	GENIC	homozygous	115812594