chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	100990278	100990279	C	T	32	GENIC	homozygous	114437747
13	100991019	100991020	A	G	26	GENIC	homozygous	114437749
13	100991268	100991269	C	A	16	GENIC	homozygous	114437751
13	100991291	100991292	A	C	15	GENIC	homozygous	114437753
13	100991442	100991443	A	G	15	GENIC	homozygous	114437755
13	100991443	100991444	G	C	15	GENIC	homozygous	114437757
13	101024473	101024474	G	A	32	GENIC	homozygous	114437759
13	101031631	101031632	G	C	31	GENIC	homozygous	114437761
13	101031634	101031635	A	T	30	GENIC	homozygous	114437763
13	101031924	101031925	G	A	37	GENIC	homozygous	114437765
13	101032161	101032162	A	G	30	GENIC	homozygous	114437767
13	101017600	101017601	C	T	34	GENIC	homozygous	114971650
13	101032162	101032163	G	A	32	GENIC	homozygous	114585097