chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59324583	59324584	C	A	5	GENIC	heterozygous	51465345
10	59326356	59326357	A	T	12	GENIC	possibly homozygous	51465347
10	59328350	59328351	T	C	18	GENIC	possibly homozygous	51465349
10	59328468	59328469	A	G	18	GENIC	possibly homozygous	52062167
10	59328939	59328940	G	A	21	GENIC	possibly homozygous	52062169
10	59329010	59329011	A	C	26	GENIC	homozygous	52062171
10	59329627	59329628	C	G	7	GENIC	possibly homozygous	51465352
10	59331551	59331552	T	C	9	GENIC	homozygous	51465355
10	59332091	59332092	T	C	25	GENIC	homozygous	51662957
10	59332407	59332408	T	TC	5	GENIC	homozygous	52062173
10	59333692	59333693	G	T	19	GENIC	homozygous	52062175
10	59334289	59334290	T	C	18	GENIC	homozygous	51465358
10	59335983	59335984	G	C	8	GENIC	homozygous	52062177
10	59336101	59336102	C	A	13	GENIC	homozygous	52062179
10	59336174	59336175	G	GACAA	12	GENIC	possibly homozygous	51465362
10	59337302	59337303	G	T	14	GENIC	possibly homozygous	51662969
10	59337857	59337858	A	G	24	GENIC	possibly homozygous	51465364
10	59338013	59338014	C	T	15	GENIC	heterozygous	52062181
10	59339162	59339163	A	G	17	GENIC	homozygous	51465365
10	59339807	59339809	GA	--	1	GENIC	homozygous	52062183
10	59345413	59345414	A	-	4	GENIC	homozygous	51465367
10	59345972	59345973	C	T	7	GENIC	homozygous	52062185
10	59346495	59346496	T	C	20	GENIC	possibly homozygous	51465368
10	59346895	59346896	C	G	30	GENIC	possibly homozygous	52062187
10	59347329	59347333	AAAT	----	14	GENIC	homozygous	52062189
10	59347638	59347639	A	-	4	GENIC	homozygous	51897448