chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	33606840	33606841	G	A	19	GENIC	homozygous	112807407
15	33607394	33607395	T	C	23	GENIC	homozygous	131168513
15	33607608	33607609	T	G	22	GENIC	homozygous	112807409
15	33611695	33611696	A	G	15	GENIC	homozygous	112807411
15	33612969	33612970	C	T	16	GENIC	heterozygous	131168514
15	33612970	33612971	A	G	16	GENIC	heterozygous	131168515
15	33612973	33612974	C	G	17	GENIC	heterozygous	131168516
15	33617591	33617592	A	G	20	GENIC	homozygous	112807413
15	33617733	33617734	T	G	23	GENIC	homozygous	112807415
15	33618723	33618724	A	G	20	GENIC	homozygous	112807417
15	33620219	33620220	C	T	18	GENIC	homozygous	112807419
15	33608412	33608413	A	G	10	GENIC	homozygous	118954727
15	33613025	33613026	T	C	19	GENIC	heterozygous	118954730
15	33613118	33613119	A	C	17	GENIC	homozygous	118954731
15	33610507	33610508	G	A	25	GENIC	homozygous	134626875
15	33614697	33614697		G	20	GENIC	homozygous	131159393
15	33620438	33620439	T	C	11	GENIC	homozygous	112879088
15	33621955	33621956	G	A	22	GENIC	homozygous	118954733
15	33623851	33623852	T	A	25	GENIC	homozygous	118954734
15	33628516	33628517	C	T	21	GENIC	homozygous	112807421
15	33628755	33628756	T	G	30	GENIC	possibly homozygous	112807423
15	33629179	33629180	T	C	26	GENIC	homozygous	112807425
15	33629533	33629534	A	G	19	GENIC	homozygous	112807427