chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31808058	31808059	T		15	GENIC	homozygous	132700624
11	31808674	31808675	T		22	GENIC	homozygous	128896271
11	31809114	31809114		T	19	GENIC	homozygous	128896272
11	31812086	31812087	T	G	19	GENIC	homozygous	115812554
11	31816607	31816608	C	T	17	GENIC	homozygous	115812558
11	31816630	31816631	T	C	18	GENIC	homozygous	115812560
11	31818999	31818999		C	18	GENIC	homozygous	132700625
11	31819852	31819853	C	G	20	GENIC	homozygous	115812568
11	31826107	31826108	T	C	28	GENIC	homozygous	115812572
11	31826979	31826980	G	A	30	GENIC	homozygous	116096994
11	31813099	31813100	C	T	25	GENIC	homozygous	116096985
11	31819202	31819203	G	A	22	GENIC	homozygous	116096988
11	31824572	31824573	A	G	21	GENIC	homozygous	116096990
11	31825714	31825715	A	C	19	GENIC	homozygous	116096992
11	31827086	31827087	T	C	30	GENIC	homozygous	115812578
11	31827405	31827406	T		22	GENIC	homozygous	132700626
11	31828379	31828380	A		20	GENIC	homozygous	128896277
11	31829285	31829286	A	C	23	GENIC	homozygous	116096996
11	31833603	31833604	T	C	28	GENIC	homozygous	115812586
11	31835047	31835047		G	14	GENIC	homozygous	132700628
11	31835049	31835050	A	C	14	GENIC	homozygous	116096998
11	31835709	31835710	T	C	26	GENIC	homozygous	115812590
11	31836429	31836430	T	C	22	GENIC	homozygous	116097000
11	31836441	31836442	G	A	21	GENIC	homozygous	115812594
11	31834188	31834189	T	C	11	GENIC	homozygous	116416052