chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	15384743	15384744	T	C	63	GENIC	homozygous	136643096
3	15385348	15385349	G	A	39	GENIC	homozygous	136643097
3	15385374	15385375	T	A	39	GENIC	homozygous	136643098
3	15386119	15386120	A	G	46	GENIC	homozygous	136643099
3	15388177	15388178	C	T	67	GENIC	homozygous	136643100
3	15388182	15388183	A	C	66	GENIC	homozygous	136643101
3	15388345	15388346	G	A	64	GENIC	homozygous	136643102
3	15389007	15389008	A	G	46	GENIC	homozygous	136643103
3	15389010	15389011	C	A	45	GENIC	homozygous	136643104
3	15389038	15389043	GAAGA		35	GENIC	homozygous	136549551
3	15389802	15389803	A		47	GENIC	homozygous	136549552
3	15391008	15391014	TCCTCT		15	GENIC	homozygous	136549553
3	15392287	15392288	T	C	57	GENIC	homozygous	136643105
3	15393394	15393395	T	C	60	GENIC	homozygous	136643106
3	15393459	15393460	T	C	50	GENIC	homozygous	136643107
3	15393582	15393583	C	T	47	GENIC	homozygous	136643108
3	15393636	15393637	T	C	65	GENIC	homozygous	136643109
3	15394698	15394699	G	C	61	GENIC	homozygous	136643110
3	15394908	15394908		GAGTAT	52	GENIC	homozygous	136549554
3	15395072	15395073	G	A	57	GENIC	homozygous	136643111
3	15395111	15395112	T	G	63	GENIC	homozygous	136643112
3	15395116	15395117	C	T	65	GENIC	homozygous	136643113
3	15395242	15395243	G	C	59	GENIC	homozygous	136643114
3	15395376	15395377	A	G	72	GENIC	homozygous	136643115
3	15395713	15395714	A	C	63	GENIC	homozygous	136643116
3	15396391	15396392	C	T	69	GENIC	homozygous	136643117
3	15398201	15398202	T	A	61	GENIC	homozygous	136643118
3	15398222	15398223	C	A	61	GENIC	homozygous	136643119
3	15398223	15398224	C	T	61	GENIC	homozygous	136643120
3	15398393	15398394	C	T	46	GENIC	possibly homozygous	136643121