chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4167981	4167982	T	C	23	GENIC	homozygous	109233193
20	4168723	4168724	G	C	30	GENIC	homozygous	109233195
20	4169029	4169030	C	T	14	GENIC	homozygous	109233196
20	4169030	4169031	A	G	14	GENIC	homozygous	109233197
20	4169062	4169063	A	C	11	GENIC	homozygous	109233198
20	4169080	4169081	C	T	9	GENIC	homozygous	109233199
20	4169124	4169125	A	C	12	GENIC	homozygous	109233200
20	4169175	4169176	T	C	15	GENIC	homozygous	109233201
20	4169190	4169191	T	C	14	GENIC	homozygous	109296021
20	4169212	4169213	C	A	12	GENIC	homozygous	109233202
20	4169217	4169218	G	T	12	GENIC	homozygous	109233203
20	4169327	4169328	G	A	18	GENIC	homozygous	109233204
20	4169335	4169336	C	T	18	GENIC	homozygous	109233205
20	4169348	4169349	C	T	15	GENIC	homozygous	109233206
20	4169522	4169523	C	A	6	GENIC	homozygous	109233207
20	4169931	4169932	A	G	19	GENIC	homozygous	109233208
20	4169935	4169936	C	T	20	GENIC	homozygous	109233209
20	4170266	4170267	C	T	24	GENIC	possibly homozygous	109233211
20	4170279	4170280	T	C	23	GENIC	possibly homozygous	109233212
20	4170281	4170282	C	A	23	GENIC	possibly homozygous	109233213
20	4170305	4170306	C	G	28	GENIC	possibly homozygous	109233214
20	4170334	4170335	A	G	32	GENIC	homozygous	109233215
20	4170413	4170414	A	G	27	GENIC	possibly homozygous	109233216