chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82147430	82147431	C	G	10	GENIC	homozygous	143460171
10	82149185	82149186	T	C	10	GENIC	homozygous	138834446
10	82149202	82149203	G	A	10	GENIC	homozygous	143460172
10	82149209	82149210	C	G	11	GENIC	homozygous	143460173
10	82149235	82149237	AC		9	GENIC	homozygous	138694696
10	82149485	82149486	T	G	14	GENIC	homozygous	143460174
10	82151093	82151094	G	A	18	GENIC	homozygous	138834448
10	82152258	82152258		AATAAC	12	GENIC	homozygous	138694697
10	82153182	82153183	T	C	6	GENIC	homozygous	154649329
10	82153182	82153183	T		6	GENIC	heterozygous	403637666
10	82155202	82155203	C	T	12	GENIC	homozygous	143460175
10	82155838	82155839	C		4	GENIC	homozygous	138694699
10	82156191	82156192	T	C	12	GENIC	homozygous	143460176
10	82158753	82158754	A	T	13	GENIC	homozygous	143460177
10	82163405	82163405		GTCGTC	11	GENIC	homozygous	138694704
10	82165248	82165249	A	T	13	GENIC	homozygous	138834458
10	82169277	82169278	G	A	17	GENIC	homozygous	143460178
10	82171235	82171236	C	G	16	GENIC	homozygous	138834462
10	82173362	82173363	A	G	14	GENIC	homozygous	138834464
10	82167537	82167538	A		13	GENIC	homozygous	143434220
10	82165592	82165592		G	13	GENIC	homozygous	143434219