chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36250370	36250370		G	34	GENIC	homozygous	148046511
10	36251287	36251287		CAAAA	29	GENIC	homozygous	148046512
10	36251948	36251949	A	C	22	GENIC	homozygous	138766364
10	36251979	36251980	T	C	23	GENIC	homozygous	148053156
10	36252314	36252315	T	C	26	GENIC	homozygous	148053157
10	36253510	36253511	A	G	28	GENIC	possibly homozygous	148053158
10	36253801	36253802	T	C	24	GENIC	possibly homozygous	148053159
10	36253822	36253823	A	T	27	GENIC	possibly homozygous	138766365
10	36254089	36254090	G	T	23	GENIC	homozygous	144866155
10	36254135	36254136	T	C	29	GENIC	homozygous	142232519
10	36255771	36255772	G	T	27	GENIC	homozygous	148053160
10	36255807	36255808	A	G	32	GENIC	homozygous	148053161
10	36256420	36256421	T	A	21	GENIC	homozygous	148053162
10	36257100	36257101	A		34	GENIC	possibly homozygous	148046513
10	36257758	36257759	G	T	37	GENIC	homozygous	148053163
10	36261537	36261538	G	T	34	GENIC	homozygous	148053164
10	36261666	36261666		G	11	GENIC	homozygous	138678836