chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	20528558	20528559	C	CAT	19	GENIC	possibly homozygous	50664667
11	20529693	20529694	T	C	27	GENIC	homozygous	50664668
11	20529971	20529972	T	G	27	GENIC	homozygous	50664669
11	20530137	20530140	TAC	---	27	GENIC	homozygous	50664671
11	20530192	20530193	A	G	36	GENIC	homozygous	50664672
11	20530260	20530261	G	T	24	GENIC	homozygous	50664673
11	20530413	20530414	T	A	25	GENIC	homozygous	50664674
11	20532050	20532051	C	T	18	GENIC	homozygous	50664677
11	20533826	20533827	A	-	34	GENIC	homozygous	51574726
11	20534562	20534563	T	-	14	GENIC	homozygous	50664680
11	20534794	20534795	C	T	18	GENIC	homozygous	51574728
11	20534998	20534999	C	T	29	GENIC	homozygous	51574730
11	20535177	20535178	T	C	25	GENIC	homozygous	50664681
11	20537473	20537474	T	C	27	GENIC	homozygous	50664682
11	20537589	20537590	G	GA	28	GENIC	homozygous	50664683
11	20538125	20538126	A	-	22	GENIC	homozygous	51574732
11	20538858	20538859	T	-	12	GENIC	possibly homozygous	51290325
11	20539084	20539085	A	AT	31	GENIC	homozygous	50664688
11	20539139	20539140	G	C	27	GENIC	homozygous	51158360
11	20539166	20539167	C	T	22	GENIC	homozygous	50664689
11	20539247	20539248	C	T	23	GENIC	homozygous	50664692
11	20539651	20539652	A	G	24	GENIC	homozygous	50664694
11	20539654	20539655	G	C	23	GENIC	homozygous	50664695
11	20539852	20539853	G	A	36	GENIC	homozygous	50664696
11	20540083	20540084	T	C	31	GENIC	homozygous	50664698
11	20540312	20540313	A	G	22	GENIC	homozygous	50664699
11	20540880	20540881	T	C	28	GENIC	homozygous	50664700
11	20541957	20541958	G	GCA	30	GENIC	homozygous	50664701
11	20542038	20542039	T	A	32	GENIC	homozygous	50664702
11	20542429	20542430	C	T	15	GENIC	homozygous	50664703
11	20542865	20542866	C	T	29	GENIC	homozygous	50664704
11	20543015	20543016	A	G	27	GENIC	homozygous	50664705
11	20543103	20543108	CGAAC	-----	28	GENIC	homozygous	50664706
11	20543380	20543381	C	T	23	GENIC	homozygous	50664708
11	20543828	20543829	C	T	3	GENIC	homozygous	51574734