chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	108396355	108396371	GTGTGTGTGTGTGTGT	----------------	5	GENIC	heterozygous	51596094
10	108396766	108396767	T	C	57	GENIC	homozygous	51596096
10	108397090	108397091	G	T	31	GENIC	homozygous	51596098
10	108397871	108397872	C	T	46	GENIC	homozygous	51596100
10	108397987	108397988	C	T	47	GENIC	homozygous	51596102
10	108398368	108398369	A	G	41	GENIC	homozygous	51596104
10	108398863	108398864	T	C	61	GENIC	homozygous	51596106
10	108399592	108399593	C	T	16	GENIC	homozygous	51596108
10	108400021	108400024	TCC	---	38	GENIC	homozygous	51596110
10	108400449	108400450	A	G	61	GENIC	homozygous	51596112
10	108401441	108401449	GTGTGTGT	--------	6	GENIC	homozygous	51596114
10	108401486	108401487	T	C	29	GENIC	possibly homozygous	51596116
10	108402283	108402284	A	G	53	GENIC	homozygous	51596118
10	108403550	108403551	T	TAAC	24	GENIC	homozygous	51596120
10	108403553	108403554	G	GGGCTAC	17	GENIC	homozygous	51596122
10	108403922	108403924	AA	--	35	GENIC	homozygous	51596124
10	108405663	108405664	T	TC	55	GENIC	homozygous	51596126
10	108406935	108406936	A	AGT	6	GENIC	homozygous	51596128
10	108407055	108407057	TT	--	10	GENIC	homozygous	51596130
10	108407879	108407880	A	T	54	GENIC	homozygous	51596132
10	108408887	108408888	T	TC	32	GENIC	heterozygous	51596134
10	108408887	108408888	T	TTC	32	GENIC	heterozygous	51596136
10	108409221	108409222	T	TCA	7	GENIC	heterozygous	51596138
10	108409485	108409486	A	G	37	GENIC	homozygous	51596140
10	108410258	108410259	T	A	40	GENIC	homozygous	51596142
10	108411238	108411239	G	A	39	GENIC	homozygous	51596144
10	108411935	108411936	C	T	20	GENIC	heterozygous	51596146
10	108412065	108412066	G	A	49	GENIC	possibly homozygous	51596148
10	108412067	108412068	C	CT	50	GENIC	homozygous	51596149
10	108412524	108412525	C	T	44	GENIC	homozygous	51596151
10	108412774	108412775	T	C	43	GENIC	homozygous	51596153
10	108412824	108412825	T	G	52	GENIC	heterozygous	51596155