chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3823634	3823635	T	C	11	GENIC	homozygous	109070071
20	3824575	3824576	G	A	27	GENIC	homozygous	109070073
20	3824582	3824583	C	A	27	GENIC	homozygous	109294650
20	3824641	3824642	C	T	24	GENIC	homozygous	109294652
20	3825553	3825554	T	C	24	GENIC	homozygous	109070075
20	3825604	3825605	T	C	19	GENIC	homozygous	109070077
20	3825935	3825936	A	G	22	GENIC	homozygous	109070079
20	3826016	3826017	G	A	25	GENIC	homozygous	109294654
20	3826094	3826095	C	T	22	GENIC	possibly homozygous	109070081
20	3826593	3826594	C	G	7	GENIC	homozygous	109294656
20	3826700	3826701	G	T	14	GENIC	homozygous	109070083
20	3826712	3826713	A	G	15	GENIC	homozygous	109070085
20	3826776	3826777	A	C	20	GENIC	homozygous	109070087
20	3827764	3827765	T	A	16	GENIC	homozygous	109294658
20	3828190	3828191	T	C	22	GENIC	homozygous	109070089