chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	40548429	40548430	A	G	59	GENIC	homozygous	130097777
20	40549099	40549100	G	A	64	GENIC	homozygous	130097778
20	40549405	40549406	G	A	67	GENIC	homozygous	130097779
20	40550902	40550902		T	52	GENIC	homozygous	129998212
20	40551375	40551380	TGTTG		20	GENIC	possibly homozygous	129998213
20	40551545	40551546	G	T	48	GENIC	homozygous	130097780
20	40551745	40551746	A	G	52	GENIC	homozygous	130097781
20	40552013	40552014	C		23	GENIC	homozygous	129998214
20	40552236	40552237	A	G	47	GENIC	homozygous	130097782
20	40553082	40553083	C	T	59	GENIC	homozygous	130097783
20	40553813	40553814	T	C	47	GENIC	possibly homozygous	130097784
20	40554123	40554123		AAAC	56	GENIC	possibly homozygous	129998215
20	40554126	40554126		AAA	57	GENIC	possibly homozygous	129998216
20	40555530	40555531	T	C	44	GENIC	homozygous	130097785
20	40556666	40556667	A		19	GENIC	homozygous	129998217
20	40556870	40556871	C	T	52	GENIC	homozygous	130097786
20	40557040	40557041	G	A	47	GENIC	homozygous	130097787
20	40557287	40557288	G	C	64	GENIC	homozygous	130097788
20	40557356	40557357	T	C	61	GENIC	homozygous	130097789
20	40557594	40557595	G	A	46	GENIC	homozygous	130097790
20	40558107	40558108	G	A	58	GENIC	homozygous	130097791
20	40559307	40559308	A	G	63	GENIC	homozygous	130097792
20	40562944	40562945	T	C	54	GENIC	homozygous	130097793
20	40563856	40563857	A	C	45	GENIC	homozygous	130097794
20	40564424	40564441	GCCGTCAGAGCGCGGTT		63	GENIC	possibly homozygous	129998218
20	40568040	40568042	CT		44	GENIC	homozygous	129998219
20	40568699	40568699		GGGTGCGTTCAGC	53	GENIC	possibly homozygous	129998220
20	40568867	40568868	A	G	60	GENIC	homozygous	130097796
20	40570904	40570905	C	T	58	GENIC	homozygous	130097797
20	40571499	40571500	T	C	60	GENIC	homozygous	130097798
20	40565979	40565980	T		11	GENIC	heterozygous	404040926
20	40565979	40565980	T	G	11	GENIC	possibly homozygous	404040925