chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	77976048	77976049	G	C	38	GENIC	homozygous	142831097
1	77977398	77977398		T	31	GENIC	homozygous	142787933
1	77978617	77978618	A	G	26	GENIC	homozygous	142831098
1	77978663	77978664	A	G	28	GENIC	homozygous	142831099
1	77978739	77978740	C	G	33	GENIC	possibly homozygous	142831100
1	77979653	77979654	A	G	27	GENIC	homozygous	142831101
1	77982047	77982048	A	C	32	GENIC	homozygous	142831102
1	77982515	77982516	A	G	27	GENIC	homozygous	142831103
1	77987772	77987773	C	A	27	GENIC	homozygous	142831104
1	77990000	77990001	A	C	23	GENIC	homozygous	142831105
1	77991128	77991128		A	25	GENIC	homozygous	142787934
1	77991899	77991900	A		26	GENIC	homozygous	142787935
1	77992048	77992049	A	G	20	GENIC	homozygous	142831106
1	77993416	77993417	A	G	10	GENIC	homozygous	142831107
1	77993434	77993435	C	G	16	GENIC	homozygous	142831108
1	77993494	77993495	A	G	29	GENIC	homozygous	142831109
1	77994130	77994131	C	T	28	GENIC	homozygous	142831110
1	77994403	77994404	T	C	25	GENIC	homozygous	142831111
1	77994566	77994567	G	A	34	GENIC	homozygous	142831112
1	77994614	77994615	G	A	32	GENIC	homozygous	142831113
1	77996128	77996129	G	A	41	GENIC	homozygous	142831114
1	77997090	77997091	T	C	33	GENIC	homozygous	142831115
1	77997578	77997579	A	C	38	GENIC	homozygous	142831116
1	77996875	77996876	T	C	35	GENIC	homozygous	143785161
1	77986142	77986143	A	C	34	GENIC	homozygous	153862126
1	77986142	77986143	A	T	34	GENIC	heterozygous	403793024
1	77993077	77993078	C	G	11	GENIC	homozygous	403793025
1	77990269	77990269		CTCACAACCATCTGT	26	GENIC	homozygous	143739750