chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	4209949	4209950	T	C	19	GENIC	homozygous	112785736
15	4213984	4213985	C	T	28	GENIC	homozygous	112785738
15	4214232	4214233	A	G	19	GENIC	homozygous	112785740
15	4217711	4217712	C	T	28	GENIC	homozygous	112785742
15	4217922	4217923	T	C	24	GENIC	homozygous	112785744
15	4219237	4219238	A	G	31	GENIC	homozygous	112785746
15	4221158	4221159	T	C	27	GENIC	homozygous	112785748
15	4222583	4222584	T	A	23	GENIC	homozygous	112785750
15	4222663	4222664	C	T	24	GENIC	homozygous	112785752
15	4223098	4223099	C	T	37	GENIC	homozygous	112785754
15	4223178	4223179	T	A	28	GENIC	homozygous	112785756
15	4223291	4223292	T	G	36	GENIC	homozygous	112785758
15	4224031	4224032	G	C	25	GENIC	homozygous	112785760
15	4224912	4224913	T	C	27	GENIC	homozygous	112785762
15	4224939	4224940	T	C	22	GENIC	homozygous	112785764
15	4227190	4227191	A	G	28	GENIC	homozygous	112785766
15	4229425	4229426	G	C	31	GENIC	homozygous	112785768
15	4229538	4229539	T	A	36	GENIC	homozygous	112785770
15	4231309	4231310	A	G	22	GENIC	homozygous	112785772
15	4232737	4232738	T	G	20	GENIC	homozygous	112785775
15	4232977	4232978	G	A	28	GENIC	homozygous	112785777
15	4235357	4235358	A	G	29	GENIC	homozygous	112785779
15	4236217	4236218	C	A	24	GENIC	heterozygous	112447645
15	4236324	4236325	T	G	37	GENIC	heterozygous	112447651