chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	89726013	89726014	G	A	15	GENIC	homozygous	114572224
13	89726240	89726241	T	C	28	GENIC	homozygous	114572226
13	89726258	89726259	G	A	33	GENIC	homozygous	114572228
13	89726601	89726602	C	T	32	GENIC	homozygous	114572230
13	89728283	89728284	G	A	43	GENIC	homozygous	114572232
13	89728524	89728525	A	G	32	GENIC	homozygous	114572234
13	89729103	89729104	G	A	46	GENIC	homozygous	114572236
13	89730202	89730203	C	T	41	GENIC	possibly homozygous	114572238
13	89730996	89730997	G	T	26	GENIC	homozygous	118503898
13	89731187	89731188	G	C	13	GENIC	heterozygous	118503899
13	89731199	89731200	A	T	12	GENIC	heterozygous	118503900
13	89731203	89731204	T	C	17	GENIC	heterozygous	118503901
13	89731214	89731215	G	T	24	GENIC	heterozygous	118503902
13	89732436	89732437	G	C	15	GENIC	possibly homozygous	115190078
13	89738441	89738442	C	G	41	GENIC	homozygous	114572240
13	89738768	89738769	G	T	36	GENIC	homozygous	114572242
13	89739724	89739725	G	T	26	GENIC	homozygous	118503903
13	89740874	89740875	T	C	33	GENIC	homozygous	114572244
13	89740981	89740982	T	G	33	GENIC	homozygous	114572246
13	89742658	89742659	A	G	18	GENIC	homozygous	114572248