chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	76978454	76978457	AGA		56	GENIC	homozygous	142787628
1	76978757	76978758	A	G	35	GENIC	homozygous	142829845
1	76978898	76978899	C	G	46	GENIC	homozygous	142829846
1	76979702	76979703	G	A	45	GENIC	homozygous	142829847
1	76979981	76979982	T	A	48	GENIC	homozygous	142829848
1	76980541	76980542	G	A	40	GENIC	homozygous	142829849
1	76981693	76981693		GGCAGA	39	GENIC	homozygous	142787629
1	76982735	76982736	A	G	49	GENIC	homozygous	142829850
1	76983842	76983843	T	C	52	GENIC	homozygous	142829851
1	76984073	76984074	A	C	41	GENIC	homozygous	142829852
1	76984542	76984543	T	A	41	GENIC	homozygous	142829853
1	76984640	76984641	C	T	45	GENIC	homozygous	142829854
1	76984766	76984767	C	G	28	GENIC	homozygous	403792816
1	76979288	76979289	C		10	GENIC	heterozygous	147893281
1	76979288	76979289	C	A	10	GENIC	homozygous	153835625
1	76984542	76984543	T		41	GENIC	heterozygous	403792814
1	76984766	76984767	C	A	28	GENIC	heterozygous	403792815
1	76984766	76984767	C		28	GENIC	heterozygous	403792817
1	76984860	76984861	A	C	27	GENIC	homozygous	142829855
1	76985139	76985140	A		32	GENIC	homozygous	403792818
1	76985139	76985140	A	G	32	GENIC	heterozygous	403792819
1	76985953	76985955	AT		43	GENIC	homozygous	142787630
1	76985984	76985985	T	C	43	GENIC	homozygous	142829856
1	76986021	76986022	C	T	41	GENIC	homozygous	142829857
1	76986143	76986144	C	G	51	GENIC	homozygous	142829858
1	76986665	76986666	A	G	51	GENIC	homozygous	142829859
1	76986864	76986864		AC	43	GENIC	homozygous	142787631
1	76986952	76986953	A	G	36	GENIC	homozygous	142829860
1	76987400	76987401	A	G	28	GENIC	homozygous	142829861
1	76989159	76989163	ACGA		35	GENIC	possibly homozygous	142787632
1	76990967	76990968	C	A	30	GENIC	homozygous	142829863
1	76991596	76991597	C	G	37	GENIC	homozygous	142829864
1	76991338	76991339	G	A	39	GENIC	homozygous	143785110
1	76991627	76991628	T	C	39	GENIC	heterozygous	147244374