chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	52294369	52294370	G	T	20	GENIC	homozygous	112682848
15	52301320	52301321	T	C	51	GENIC	homozygous	112508933
15	52302295	52302295		AC	43	GENIC	heterozygous	130149437
15	52302302	52302303	A	G	46	GENIC	heterozygous	124077179
15	52302308	52302308		A	48	GENIC	heterozygous	130149438
15	52302310	52302313	CTG		48	GENIC	heterozygous	130149439
15	52302313	52302314	C	A	47	GENIC	heterozygous	124077182
15	52302319	52302319		G	40	GENIC	heterozygous	130149440
15	52302321	52302322	C	G	41	GENIC	heterozygous	124077184
15	52302323	52302324	A	T	40	GENIC	heterozygous	124077185
15	52302324	52302325	C	G	40	GENIC	heterozygous	124077186
15	52302328	52302329	G	C	39	GENIC	heterozygous	124077187
15	52302330	52302331	A	G	38	GENIC	heterozygous	124077188
15	52302362	52302363	G	A	57	GENIC	heterozygous	119060397
15	52302446	52302447	A	C	51	GENIC	heterozygous	124077189
15	52304897	52304897		A	15	GENIC	possibly homozygous	133500743
15	52305952	52305953	G	T	47	GENIC	homozygous	112508937
15	52309054	52309055	G	A	42	GENIC	homozygous	112682850
15	52313712	52313713	A	G	53	GENIC	homozygous	112682852
15	52315581	52315582	T	C	44	GENIC	homozygous	112508943
15	52318487	52318487		A	38	GENIC	possibly homozygous	129256149
15	52302455	52302456	G	A	48	GENIC	heterozygous	130791109