chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	106845394	106845395	A	T	29	GENIC	possibly homozygous	138409184
8	106846117	106846118	A	G	22	GENIC	homozygous	147279977
8	106847097	106847098	C	T	24	GENIC	homozygous	138409186
8	106847660	106847661	G	A	13	GENIC	homozygous	138409187
8	106848010	106848011	T	C	29	GENIC	homozygous	138409189
8	106848712	106848713	G	A	24	GENIC	homozygous	138409190
8	106849563	106849564	T	C	22	GENIC	homozygous	147279978
8	106849882	106849883	A	G	15	GENIC	homozygous	142098967
8	106850072	106850073	G	A	13	GENIC	homozygous	142098968
8	106850107	106850108	G	A	8	GENIC	homozygous	142098969
8	106850117	106850118	T	C	9	GENIC	homozygous	142098970
8	106850152	106850153	A	G	10	GENIC	homozygous	142098971
8	106850372	106850373	A	G	21	GENIC	homozygous	138409192
8	106850397	106850398	A	T	23	GENIC	homozygous	142098972
8	106850530	106850531	T	G	21	GENIC	homozygous	142098973
8	106850591	106850592	G	A	19	GENIC	homozygous	142098974
8	106850659	106850660	T	G	22	GENIC	homozygous	138409193
8	106850666	106850667	G	T	23	GENIC	homozygous	142098975
8	106850789	106850790	T	C	16	GENIC	homozygous	142098976
8	106852098	106852099	A	T	12	GENIC	homozygous	142098979
8	106852243	106852244	T	C	13	GENIC	homozygous	142098980
8	106853057	106853058	G	A	22	GENIC	homozygous	142098981
8	106853250	106853251	T	C	11	GENIC	homozygous	147279979
8	106853600	106853601	T	A	27	GENIC	homozygous	138409194
8	106854335	106854336	C	T	33	GENIC	homozygous	138409195
8	106854684	106854685	T	A	19	GENIC	homozygous	147279980
8	106856848	106856849	A	T	14	GENIC	homozygous	138409196
8	106857747	106857748	G	C	22	GENIC	homozygous	142098983
8	106850189	106850191	TG		11	GENIC	homozygous	142030124
8	106852284	106852284		GAA	12	GENIC	homozygous	142030125
8	106853238	106853238		TAA	12	GENIC	homozygous	138263079