chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	108396469	108396470	A	G	27	GENIC	homozygous	51953747
10	108396766	108396767	T	C	16	GENIC	possibly homozygous	51596096
10	108396843	108396844	G	A	17	GENIC	possibly homozygous	51953750
10	108397090	108397091	G	T	11	GENIC	possibly homozygous	51596098
10	108397341	108397342	T	C	22	GENIC	possibly homozygous	51953753
10	108397389	108397390	G	A	25	GENIC	possibly homozygous	51953756
10	108398923	108398924	C	T	13	GENIC	homozygous	51953759
10	108399390	108399391	A	G	19	GENIC	possibly homozygous	51953762
10	108399592	108399593	C	T	15	GENIC	possibly homozygous	51596108
10	108400014	108400015	C	CTCT	2	GENIC	homozygous	51953766
10	108400065	108400066	C	A	8	GENIC	homozygous	51953772
10	108401443	108401451	GTGTGTGT	--------	1	GENIC	homozygous	52331693
10	108401486	108401487	T	C	12	GENIC	possibly homozygous	51596116
10	108402283	108402284	A	G	22	GENIC	possibly homozygous	51596118
10	108403425	108403426	G	A	16	GENIC	possibly homozygous	51953778
10	108403550	108403551	T	TAAC	1	GENIC	homozygous	51596120
10	108403553	108403554	G	GGGCTAC	1	GENIC	homozygous	51596122
10	108405663	108405664	T	TC	25	GENIC	possibly homozygous	51596126
10	108407056	108407057	T	-	5	GENIC	heterozygous	52447870
10	108407067	108407068	T	G	7	GENIC	heterozygous	52734366
10	108407071	108407072	T	G	7	GENIC	heterozygous	52271553
10	108407075	108407076	T	G	3	GENIC	heterozygous	52271555
10	108409485	108409486	A	G	21	GENIC	homozygous	51596140
10	108411969	108411970	C	CACACACACACACACACACAT	9	GENIC	possibly homozygous	52331695
10	108412067	108412068	C	CT	14	GENIC	homozygous	51596149
10	108412524	108412525	C	T	29	GENIC	possibly homozygous	51596151
10	108412774	108412775	T	C	26	GENIC	homozygous	51596153