chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82146887	82146888	G	A	11	GENIC	heterozygous	149056783
10	82147430	82147431	C	G	51	GENIC	homozygous	143460171
10	82149185	82149186	T	C	39	GENIC	homozygous	138834446
10	82149202	82149203	G	A	30	GENIC	homozygous	143460172
10	82149209	82149210	C	G	30	GENIC	homozygous	143460173
10	82149235	82149237	AC		27	GENIC	homozygous	138694696
10	82149485	82149486	T	G	45	GENIC	homozygous	143460174
10	82151093	82151094	G	A	28	GENIC	homozygous	138834448
10	82152258	82152258		AATAAC	35	GENIC	homozygous	138694697
10	82155202	82155203	C	T	50	GENIC	possibly homozygous	143460175
10	82155838	82155839	C		18	GENIC	possibly homozygous	138694699
10	82156191	82156192	T	C	31	GENIC	homozygous	143460176
10	82158753	82158754	A	T	32	GENIC	homozygous	143460177
10	82163405	82163405		GTCGTC	16	GENIC	homozygous	138694704
10	82165248	82165249	A	T	40	GENIC	homozygous	138834458
10	82169277	82169278	G	A	65	GENIC	homozygous	143460178
10	82171235	82171236	C	G	54	GENIC	homozygous	138834462
10	82173362	82173363	A	G	27	GENIC	homozygous	138834464
10	82167537	82167538	A		36	GENIC	homozygous	143434220
10	82153182	82153183	T	C	11	GENIC	homozygous	154649329
10	82153182	82153183	T		11	GENIC	heterozygous	403637666
10	82165592	82165592		G	33	GENIC	possibly homozygous	143434219