chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91133094	91133095	C	T	22	GENIC	homozygous	117068583
10	91134392	91134393	A	G	17	GENIC	homozygous	116905425
10	91134557	91134558	C	T	11	GENIC	homozygous	116905427
10	91134900	91134901	T	A	15	GENIC	homozygous	116905429
10	91135716	91135717	A	G	17	GENIC	homozygous	116905431
10	91136156	91136157	A	G	11	GENIC	homozygous	116905433
10	91141239	91141240	T	C	13	GENIC	homozygous	116905439
10	91146554	91146555	T	C	13	GENIC	homozygous	116905441
10	91147362	91147363	A	G	14	GENIC	homozygous	116905443
10	91149470	91149471	A	G	16	GENIC	homozygous	116905445
10	91149559	91149560	A	T	11	GENIC	homozygous	116905447
10	91149579	91149580	T	C	9	GENIC	homozygous	116905449
10	91150735	91150736	T	C	14	GENIC	homozygous	116905451
10	91152040	91152041	C	T	19	GENIC	homozygous	116905453
10	91158060	91158061	G	T	14	GENIC	heterozygous	117068585
10	91159672	91159673	T	C	23	GENIC	homozygous	116905457
10	91159801	91159802	G	A	19	GENIC	homozygous	116905459
10	91160311	91160312	A	G	9	GENIC	homozygous	116905461