chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	61066618	61066619	A	T	24	GENIC	homozygous	115219420
13	61066721	61066722	T	C	13	GENIC	homozygous	114366555
13	61067050	61067051	G	T	7	GENIC	homozygous	126147053
13	61067158	61067159	A	G	19	GENIC	homozygous	115219422
13	61067193	61067194	A	G	16	GENIC	homozygous	115219424
13	61067561	61067562	C	T	5	GENIC	homozygous	115219426
13	61068064	61068065	T	C	4	GENIC	homozygous	115219428
13	61068666	61068667	C	T	9	GENIC	homozygous	115219430
13	61068685	61068686	G	A	7	GENIC	homozygous	115219432
13	61069131	61069132	A	C	9	GENIC	homozygous	114366556
13	61069367	61069368	G	A	9	GENIC	homozygous	114366558
13	61069469	61069470	A	G	7	GENIC	homozygous	114366559
13	61069481	61069482	G	C	7	GENIC	homozygous	114366560
13	61069514	61069515	T	G	11	GENIC	homozygous	114366561
13	61069581	61069582	A	G	14	GENIC	homozygous	114366562
13	61069600	61069601	T	C	13	GENIC	homozygous	114366563
13	61069838	61069839	T	C	11	GENIC	homozygous	114366564