chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	61066721	61066722	T	C	24	GENIC	possibly homozygous	114366555
13	61068321	61068322	A	G	23	GENIC	homozygous	114625896
13	61069131	61069132	A	C	19	GENIC	homozygous	114366556
13	61069360	61069361	A	C	25	GENIC	homozygous	114366557
13	61069367	61069368	G	A	26	GENIC	homozygous	114366558
13	61069374	61069375	A		25	GENIC	homozygous	129061830
13	61069469	61069470	A	G	23	GENIC	homozygous	114366559
13	61069481	61069482	G	C	22	GENIC	homozygous	114366560
13	61069514	61069515	T	G	23	GENIC	homozygous	114366561
13	61069581	61069582	A	G	27	GENIC	homozygous	114366562
13	61069600	61069601	T	C	27	GENIC	homozygous	114366563
13	61069838	61069839	T	C	18	GENIC	homozygous	114366564