chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10377492	10377493	T	-	7	GENIC	heterozygous	51616509
10	10383564	10383565	C	CTTTT	9	GENIC	heterozygous	51324638
10	10402719	10402720	C	-	16	GENIC	homozygous	51324669
10	10402721	10402722	C	-	16	GENIC	homozygous	51324670
10	10402728	10402729	C	-	20	GENIC	homozygous	51324672
10	10402828	10402954	AGTGTGCCCCAGATGTTGTGCTATCGTGTTCTGGCTTCAGTGACTTACTTTCTCAGGGTTAATTTAAGCTTTTGTCTTTGCAGGCTTTCATTAAAGTGGTGATCTCTTGGAAGAGGTTATATATTT	------------------------------------------------------------------------------------------------------------------------------	20	GENIC	homozygous	52312846
10	10416836	10416837	C	CTTTT	6	GENIC	heterozygous	52355138
10	10416858	10416860	GG	--	17	GENIC	heterozygous	52355140
10	10416859	10416860	G	GTTTTTTTTTTT	16	GENIC	heterozygous	52355142
10	10419250	10419251	G	-	26	GENIC	homozygous	51324714
10	10419252	10419253	G	GT	26	GENIC	homozygous	52355146
10	10420393	10420394	G	T	15	GENIC	homozygous	51324717
10	10420441	10420442	A	C	12	GENIC	homozygous	51324718
10	10420511	10420512	A	C	16	GENIC	homozygous	51324720
10	10434091	10434092	C	-	4	GENIC	heterozygous	52646247
10	10438696	10438697	A	ACAAAAT	29	GENIC	homozygous	51324743
10	10440588	10440589	G	GT	22	GENIC	homozygous	51324746
10	10448813	10448814	C	-	4	GENIC	homozygous	51324758
10	10448829	10448830	A	AC	3	GENIC	homozygous	51324759
10	10454203	10454204	C	CTTTTTTTTTTTT	16	GENIC	heterozygous	52355156