chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3917786	3917787	C	-	28	GENIC	homozygous	45374039
20	3917795	3917796	T	C	27	GENIC	homozygous	45374040
20	3918010	3918011	A	T	32	GENIC	homozygous	45374041
20	3918032	3918033	A	G	32	GENIC	homozygous	45374042
20	3918197	3918198	G	A	27	GENIC	homozygous	45374043
20	3918363	3918364	T	C	26	GENIC	homozygous	45374044
20	3918705	3918706	T	TG	41	GENIC	homozygous	45374045
20	3918707	3918708	T	C	41	GENIC	homozygous	45374046
20	3918731	3918732	T	C	30	GENIC	homozygous	45374047
20	3918760	3918761	T	C	27	GENIC	homozygous	45374048
20	3918991	3918992	C	T	34	GENIC	homozygous	45374049
20	3918998	3918999	T	C	38	GENIC	homozygous	45374050
20	3919018	3919019	A	G	37	GENIC	homozygous	45374051
20	3919025	3919026	A	G	37	GENIC	homozygous	45374052
20	3919058	3919059	G	A	32	GENIC	homozygous	45374053
20	3919064	3919065	T	C	29	GENIC	homozygous	45374054
20	3919240	3919241	G	T	25	GENIC	homozygous	45374055
20	3919358	3919359	A	G	28	GENIC	homozygous	45374056
20	3919548	3919549	G	A	21	GENIC	homozygous	45374057
20	3919552	3919553	T	C	21	GENIC	homozygous	45374058