chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	113400744	113400745	C	T	39	GENIC	homozygous	111677291
3	113401549	113401550	T	C	39	GENIC	homozygous	111677292
3	113401652	113401653	C	T	40	GENIC	homozygous	112139855
3	113401663	113401669	TCTGTC		38	GENIC	homozygous	127919657
3	113401734	113401735	C	T	50	GENIC	homozygous	111677293
3	113403342	113403343	T	C	47	GENIC	homozygous	111677294
3	113403358	113403359	C	G	38	GENIC	homozygous	111677295
3	113403541	113403541		T	8	GENIC	possibly homozygous	127919658
3	113403559	113403559		TG	4	GENIC	heterozygous	132392857
3	113404621	113404622	G	A	38	GENIC	homozygous	111677296
3	113404637	113404638	G	A	40	GENIC	homozygous	111677297
3	113404655	113404656	G	T	39	GENIC	homozygous	111677298
3	113405291	113405292	G	T	48	GENIC	homozygous	111677299
3	113403560	113403560		G	3	GENIC	heterozygous	130908318