chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	89762632	89762633	G	GAAGCCCCTAAAGAGAAACCTCCCTACCACCCTCCCCAACCCA	16	GENIC	homozygous	51192746
11	89762800	89762801	A	G	19	GENIC	homozygous	51134016
11	89763233	89763234	T	G	20	GENIC	homozygous	51134019
11	89763309	89763310	C	CCAGG	9	GENIC	homozygous	51134022
11	89763696	89763697	A	G	24	GENIC	homozygous	51134025
11	89764160	89764161	G	A	24	GENIC	homozygous	51134028
11	89764800	89764801	A	C	30	GENIC	possibly homozygous	51134031
11	89764907	89764908	C	T	32	GENIC	homozygous	51134033
11	89764913	89764914	T	C	31	GENIC	homozygous	51134036
11	89765029	89765030	G	A	24	GENIC	homozygous	51134038
11	89765218	89765219	G	T	30	GENIC	homozygous	51134041
11	89765263	89765264	C	T	28	GENIC	homozygous	51134045
11	89765305	89765306	T	C	28	GENIC	homozygous	51134048
11	89765498	89765499	C	T	31	GENIC	homozygous	51134051
11	89766328	89766329	A	G	10	GENIC	homozygous	51034637
11	89768753	89768754	T	C	24	GENIC	homozygous	51134066
11	89769677	89769678	G	A	18	GENIC	homozygous	51134071
11	89769791	89769792	T	C	27	GENIC	homozygous	51134074
11	89777460	89777461	C	-	2	GENIC	heterozygous	50862970
11	89788602	89788603	C	CGT	5	GENIC	heterozygous	51280356
11	89805708	89805709	G	GCA	2	GENIC	homozygous	50862971
11	89808434	89808435	G	GTA	2	GENIC	homozygous	50862973
11	89809498	89809499	T	-	10	GENIC	homozygous	51192756