chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	11725291	11725292	G	T	43	GENIC	homozygous	116495335
10	11725577	11725578	G	C	29	GENIC	homozygous	116495337
10	11725899	11725900	G	C	43	GENIC	homozygous	116495339
10	11726840	11726841	G	A	32	GENIC	homozygous	116495341
10	11726856	11726857	C	A	35	GENIC	homozygous	116495343
10	11729903	11729904	G	A	26	GENIC	homozygous	116495345
10	11732330	11732331	C	T	44	GENIC	homozygous	116495347
10	11732827	11732828	G	C	29	GENIC	homozygous	116495349
10	11734826	11734827	C	T	38	GENIC	homozygous	116495351
10	11736722	11736723	G	T	30	GENIC	homozygous	116495353
10	11744399	11744400	A	G	26	GENIC	homozygous	116495355
10	11745814	11745815	T	C	23	GENIC	homozygous	116495357
10	11745827	11745828	T	G	26	GENIC	homozygous	116495359
10	11747302	11747303	T	C	30	GENIC	homozygous	116495361
10	11748710	11748711	G	A	30	GENIC	homozygous	116495363
10	11749510	11749511	T	G	33	GENIC	homozygous	116495365
10	11752717	11752718	A	G	47	GENIC	homozygous	116495367
10	11756255	11756256	A	G	39	GENIC	homozygous	116495369
10	11757029	11757030	A	C	30	GENIC	homozygous	116495371
10	11757452	11757453	T	C	29	GENIC	homozygous	116495373