chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	89726258	89726259	G	A	5	GENIC	homozygous	114572228
13	89727003	89727004	C	T	8	GENIC	homozygous	115222526
13	89727289	89727290	C	T	11	GENIC	homozygous	115190072
13	89728199	89728200	A	G	8	GENIC	homozygous	115190074
13	89728283	89728284	G	A	8	GENIC	homozygous	114572232
13	89728524	89728525	A	G	8	GENIC	homozygous	114572234
13	89728997	89728998	A	G	4	GENIC	homozygous	115222528
13	89729103	89729104	G	A	5	GENIC	homozygous	114572236
13	89730067	89730068	G	A	5	GENIC	homozygous	115190076
13	89731038	89731039	T	A	2	GENIC	homozygous	115222530
13	89733523	89733524	A	G	3	GENIC	homozygous	115222532
13	89735314	89735315	T	C	2	GENIC	homozygous	115190080
13	89736067	89736068	G	C	11	GENIC	homozygous	115190082
13	89736970	89736971	A	T	5	GENIC	homozygous	115222534
13	89738441	89738442	C	G	5	GENIC	homozygous	114572240
13	89740874	89740875	T	C	4	GENIC	homozygous	114572244
13	89740981	89740982	T	G	3	GENIC	homozygous	114572246
13	89741383	89741384	C	G	7	GENIC	homozygous	115190084
13	89742437	89742438	C	T	8	GENIC	homozygous	115190086
13	89743353	89743354	C	T	13	GENIC	homozygous	115190087