chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	4214232	4214233	A	G	54	GENIC	homozygous	112785740
15	4216044	4216045	T	C	40	GENIC	homozygous	113118655
15	4217922	4217923	T	C	58	GENIC	possibly homozygous	112785744
15	4219237	4219238	A	G	42	GENIC	homozygous	112785746
15	4219545	4219545		T	48	GENIC	homozygous	131155268
15	4224904	4224905	C	G	47	GENIC	possibly homozygous	113118658
15	4224939	4224940	T	C	41	GENIC	possibly homozygous	112785764
15	4224944	4224952	TGCTTCCA		39	GENIC	possibly homozygous	131155269
15	4227190	4227191	A	G	46	GENIC	homozygous	112785766
15	4231309	4231310	A	G	55	GENIC	homozygous	112785772
15	4232737	4232738	T	G	64	GENIC	homozygous	112785775
15	4236154	4236155	C	T	56	GENIC	heterozygous	112447643
15	4236217	4236218	C	A	56	GENIC	heterozygous	112447645
15	4236260	4236261	C	T	56	GENIC	heterozygous	112447647
15	4236266	4236267	T	G	52	GENIC	heterozygous	112447649
15	4236324	4236325	T	G	69	GENIC	heterozygous	112447651
15	4236375	4236376	G	A	74	GENIC	heterozygous	112447653
15	4236392	4236393	C	A	74	GENIC	heterozygous	112447655
15	4236393	4236394	T	C	74	GENIC	heterozygous	112447657
15	4236400	4236401	T	C	75	GENIC	heterozygous	112447659
15	4236437	4236438	C	T	83	GENIC	heterozygous	112447661
15	4236464	4236465	G	A	79	GENIC	heterozygous	112447663
15	4236468	4236469	A	T	80	GENIC	heterozygous	112447665
15	4236483	4236484	G	A	75	GENIC	heterozygous	112447667
15	4236494	4236495	C	T	73	GENIC	heterozygous	112447669
15	4236650	4236651	G	A	51	GENIC	homozygous	113118660
15	4236178	4236178		TG	45	GENIC	heterozygous	129225245
15	4236568	4236569	T		56	GENIC	heterozygous	129225246
15	4236370	4236372	TC		73	GENIC	heterozygous	130591836
15	4236549	4236550	C	T	56	GENIC	heterozygous	113224739
15	4236550	4236551	T	C	56	GENIC	heterozygous	113224740
15	4236609	4236610	T	C	55	GENIC	homozygous	118860341