chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	108596292	108596293	G	A	20	GENIC	homozygous	138411601
8	108598125	108598126	A	G	18	GENIC	homozygous	138411602
8	108598133	108598134	A	C	18	GENIC	homozygous	138411603
8	108598596	108598597	T	A	18	GENIC	homozygous	142099598
8	108600549	108600550	A	G	27	GENIC	homozygous	138411604
8	108600648	108600651	TCT		19	GENIC	possibly homozygous	138263693
8	108600845	108600846	T	C	19	GENIC	homozygous	142099599
8	108600905	108600906	G	A	25	GENIC	homozygous	142099600
8	108601814	108601815	G	T	30	GENIC	homozygous	138411605
8	108601930	108601931	T	C	25	GENIC	homozygous	142099601
8	108601956	108601957	A	G	28	GENIC	homozygous	142099602
8	108601958	108601959	A	G	28	GENIC	homozygous	142099603
8	108602388	108602389	C	G	16	GENIC	homozygous	142099604
8	108603280	108603281	T	G	22	GENIC	homozygous	142099605
8	108604653	108604654	T	C	15	GENIC	homozygous	142099606
8	108604656	108604657	G	A	15	GENIC	homozygous	142099607
8	108607907	108607908	T	C	27	GENIC	homozygous	142099608
8	108610210	108610211	A	G	21	GENIC	homozygous	138411607
8	108610278	108610279	C	T	21	GENIC	homozygous	142099609
8	108610474	108610475	C	T	29	GENIC	homozygous	142099610