chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	121396943	121396945	TC	--	4	GENIC	heterozygous	52157146
9	121397430	121397431	A	-	19	GENIC	homozygous	52157148
9	121398605	121398606	C	CT	20	GENIC	possibly homozygous	52157150
9	121399145	121399146	C	T	27	GENIC	homozygous	52157152
9	121399894	121399895	T	C	22	GENIC	homozygous	52157154
9	121401763	121401764	C	A	26	GENIC	homozygous	52157156
9	121404994	121404995	G	A	34	GENIC	homozygous	52157158
9	121405787	121405788	A	C	31	GENIC	homozygous	52157160
9	121405887	121405888	C	CAA	22	GENIC	homozygous	52157162
9	121406287	121406288	T	G	22	GENIC	homozygous	52157164
9	121406360	121406361	C	T	20	GENIC	homozygous	52157166
9	121407608	121407613	TGTGT	-----	7	GENIC	heterozygous	52157168
9	121407608	121407611	TGT	---	7	GENIC	heterozygous	52157170
9	121409836	121409837	T	-	18	GENIC	homozygous	52157174
9	121410099	121410100	G	A	13	GENIC	homozygous	52157176
9	121411196	121411197	C	A	30	GENIC	homozygous	52157178
9	121404406	121404414	TATGTATG	--------	3	GENIC	homozygous	53194992
9	121406343	121406344	T	TTGTGTG	9	GENIC	homozygous	53194993