chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	32607029	32607030	C	CTGTG	4	GENIC	homozygous	45524495
20	32608832	32608833	C	T	13	GENIC	heterozygous	45524502
20	32608836	32608837	C	T	13	GENIC	heterozygous	45524504
20	32608840	32608841	C	T	14	GENIC	heterozygous	45524506
20	32614304	32614308	CACA	----	14	GENIC	heterozygous	45524516
20	32617116	32617117	C	T	11	GENIC	heterozygous	45524522
20	32619887	32619889	AC	--	10	GENIC	heterozygous	45524532
20	32621415	32621416	C	-	22	GENIC	homozygous	45524542
20	32621702	32621703	C	-	15	GENIC	heterozygous	45524543
20	32621750	32621751	C	T	7	GENIC	heterozygous	45524545
20	32623508	32623510	CT	--	9	GENIC	heterozygous	45703746
20	32641206	32641207	A	AG	16	GENIC	heterozygous	45524569
20	32641207	32641208	A	G	21	GENIC	possibly homozygous	45524571
20	32655525	32655527	CA	--	22	GENIC	heterozygous	45703875
20	32658547	32658548	T	-	1	GENIC	homozygous	45524597
20	32662500	32662503	AAA	---	7	GENIC	heterozygous	45524611
20	32663934	32663935	G	A	33	GENIC	heterozygous	45524621
20	32676636	32676637	G	GA	12	GENIC	heterozygous	45703885
20	32609862	32609866	ACAC	----	3	GENIC	heterozygous	45742508
20	32665359	32665361	TG	--	10	GENIC	heterozygous	45742509
20	32662499	32662500	G	GA	7	GENIC	heterozygous	45625000