chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	40548429	40548430	A	G	53	GENIC	homozygous	130097777
20	40549099	40549100	G	A	47	GENIC	homozygous	130097778
20	40549405	40549406	G	A	56	GENIC	homozygous	130097779
20	40550902	40550902		T	51	GENIC	homozygous	129998212
20	40551375	40551380	TGTTG		18	GENIC	heterozygous	129998213
20	40551545	40551546	G	T	38	GENIC	homozygous	130097780
20	40551745	40551746	A	G	47	GENIC	homozygous	130097781
20	40552013	40552014	C		29	GENIC	homozygous	129998214
20	40552236	40552237	A	G	46	GENIC	homozygous	130097782
20	40553082	40553083	C	T	52	GENIC	homozygous	130097783
20	40553813	40553814	T	C	40	GENIC	homozygous	130097784
20	40554123	40554123		AAAC	45	GENIC	homozygous	129998215
20	40554126	40554126		AAA	46	GENIC	homozygous	129998216
20	40555530	40555531	T	C	43	GENIC	homozygous	130097785
20	40556666	40556667	A		19	GENIC	homozygous	129998217
20	40556870	40556871	C	T	45	GENIC	homozygous	130097786
20	40557040	40557041	G	A	43	GENIC	homozygous	130097787
20	40557287	40557288	G	C	53	GENIC	homozygous	130097788
20	40557356	40557357	T	C	48	GENIC	homozygous	130097789
20	40557594	40557595	G	A	58	GENIC	homozygous	130097790
20	40558107	40558108	G	A	50	GENIC	homozygous	130097791
20	40559307	40559308	A	G	61	GENIC	homozygous	130097792
20	40562944	40562945	T	C	52	GENIC	homozygous	130097793
20	40563856	40563857	A	C	53	GENIC	homozygous	130097794
20	40564424	40564441	GCCGTCAGAGCGCGGTT		55	GENIC	homozygous	129998218
20	40568040	40568042	CT		41	GENIC	homozygous	129998219
20	40568699	40568699		GGGTGCGTTCAGC	43	GENIC	homozygous	129998220
20	40568867	40568868	A	G	44	GENIC	homozygous	130097796
20	40570904	40570905	C	T	51	GENIC	homozygous	130097797
20	40571499	40571500	T	C	41	GENIC	homozygous	130097798
20	40565979	40565980	T		9	GENIC	heterozygous	404040926
20	40565979	40565980	T	G	9	GENIC	heterozygous	404040925