chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89181148	89181149	T	G	31	GENIC	homozygous	116675224
10	89181273	89181274	C	T	45	GENIC	homozygous	116902220
10	89182800	89182806	GAGGGA		30	GENIC	homozygous	131902678
10	89183531	89183532	A	T	26	GENIC	heterozygous	130683895
10	89183536	89183537	A	T	29	GENIC	heterozygous	132491211
10	89183546	89183547	T	C	33	GENIC	homozygous	116819612
10	89184243	89184244	A	G	48	GENIC	homozygous	116819614
10	89186088	89186089	C	G	47	GENIC	homozygous	116902222
10	89186798	89186799	C	T	33	GENIC	possibly homozygous	116819616
10	89188528	89188528		TG	33	GENIC	homozygous	131902680
10	89188599	89188600	C		13	GENIC	homozygous	128843652
10	89188959	89188960	T	C	41	GENIC	homozygous	116819618
10	89189512	89189513	C	T	30	GENIC	homozygous	116902224
10	89193931	89193932	C	T	32	GENIC	homozygous	116902226
10	89194593	89194594	T	A	30	GENIC	homozygous	116819628
10	89195093	89195093		A	14	GENIC	homozygous	128843653
10	89195128	89195128		T	13	GENIC	homozygous	128843654
10	89195192	89195193	C		12	GENIC	homozygous	131902681
10	89195208	89195209	A		10	GENIC	homozygous	128843655
10	89195248	89195249	C		12	GENIC	homozygous	128843656
10	89195254	89195255	C		13	GENIC	homozygous	128843657
10	89195694	89195695	T	C	40	GENIC	homozygous	116819632
10	89196830	89196831	A	G	45	GENIC	homozygous	116819634
10	89195130	89195131	C	A	14	GENIC	homozygous	117068438