chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	32607029	32607030	C	CTG	12	GENIC	heterozygous	45881769
20	32607030	32607032	TG	--	12	GENIC	heterozygous	45703743
20	32611962	32611963	C	CAGGGGTTGGGGATTTGGCTCAGTGGTAGAGCGCTTGCCAAGGAAGCGCAAGGCCCTGGGTTTGGTCCCCAGCTCCGAAAAAAAAAA	18	GENIC	homozygous	45847045
20	32614308	32614310	CA	--	8	GENIC	heterozygous	45847046
20	32617086	32617087	T	-	2	GENIC	heterozygous	45881776
20	32617420	32617422	TG	--	3	GENIC	heterozygous	45847048
20	32621411	32621412	C	G	3	GENIC	homozygous	45524536
20	32621412	32621413	C	G	2	GENIC	homozygous	45524538
20	32621413	32621414	C	G	2	GENIC	homozygous	45524540
20	32621415	32621416	C	-	2	GENIC	homozygous	45524542
20	32623507	32623508	A	ACTCTCTCT	1	GENIC	homozygous	45857185
20	32625010	32625011	A	AGTCGGG	36	GENIC	heterozygous	45822272
20	32637909	32637911	AC	--	2	GENIC	heterozygous	45881778
20	32640781	32640782	G	GT	10	GENIC	heterozygous	45859746
20	32646221	32646223	AC	--	14	GENIC	heterozygous	45857186
20	32655525	32655527	CA	--	25	GENIC	heterozygous	45703875
20	32656619	32656623	ACAC	----	8	GENIC	heterozygous	45857187
20	32656621	32656623	AC	--	8	GENIC	heterozygous	45847049
20	32658547	32658548	T	-	10	GENIC	heterozygous	45524597
20	32665639	32665640	A	-	8	GENIC	heterozygous	45847051