chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	41574536	41574537	A	G	11	GENIC	homozygous	51067564
11	41574674	41574675	T	G	14	GENIC	homozygous	51067566
11	41574720	41574721	A	G	14	GENIC	homozygous	51067568
11	41574746	41574747	A	-	16	GENIC	homozygous	51067570
11	41575070	41575071	T	A	17	GENIC	homozygous	51067572
11	41575105	41575106	T	C	20	GENIC	homozygous	51067574
11	41575252	41575253	A	G	16	GENIC	possibly homozygous	51067576
11	41576033	41576034	A	G	21	GENIC	homozygous	51067578
11	41576036	41576037	C	CCA	21	GENIC	homozygous	51067580
11	41576570	41576571	A	G	15	GENIC	homozygous	51067582
11	41576681	41576682	C	T	15	GENIC	homozygous	51067584
11	41576839	41576840	A	C	13	GENIC	homozygous	51067586
11	41577806	41577807	T	C	14	GENIC	homozygous	50750143
11	41577924	41577925	A	G	17	GENIC	homozygous	51067588
11	41578158	41578159	T	C	19	GENIC	homozygous	51067590
11	41578172	41578173	T	G	18	GENIC	homozygous	50750144
11	41583424	41583425	G	A	12	GENIC	homozygous	50750156
11	41608112	41608113	G	A	14	GENIC	homozygous	50750267
11	41608231	41608232	A	-	10	GENIC	homozygous	50750279
11	41608237	41608238	C	T	10	GENIC	homozygous	50750280
11	41608244	41608245	G	T	10	GENIC	homozygous	50750281
11	41608247	41608248	G	T	10	GENIC	homozygous	50750282
11	41608254	41608255	C	T	10	GENIC	homozygous	50750283
11	41608260	41608261	C	T	10	GENIC	homozygous	50750284