chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	32046833	32046834	A	T	61	GENIC	homozygous	139503149
14	32047447	32047448	C	T	57	GENIC	homozygous	139503150
14	32048147	32048148	T	C	34	GENIC	homozygous	139503151
14	32048515	32048516	G	A	36	GENIC	homozygous	139503152
14	32048648	32048649	T	C	51	GENIC	possibly homozygous	139503153
14	32048956	32048957	C	T	52	GENIC	homozygous	139503154
14	32049492	32049493	G	A	58	GENIC	homozygous	139503155
14	32049624	32049625	T	G	73	GENIC	homozygous	139503156
14	32050257	32050258	C	T	38	GENIC	homozygous	139503157
14	32050258	32050259	T	G	40	GENIC	homozygous	139503158
14	32052616	32052617	G	A	49	GENIC	homozygous	139503159
14	32052699	32052700	A	G	32	GENIC	homozygous	139503160
14	32048291	32048291		T	26	GENIC	possibly homozygous	139390308
14	32050207	32050207		ACAGCC	32	GENIC	homozygous	139390309
14	32056318	32056322	TTCT		26	GENIC	homozygous	139390310
14	32057291	32057291		AC	56	GENIC	homozygous	139390311
14	32058124	32058125	G	A	43	GENIC	homozygous	139503161
14	32058914	32058915	T	C	59	GENIC	homozygous	139503162
14	32059170	32059171	C	G	60	GENIC	homozygous	139503163
14	32059478	32059479	A	G	55	GENIC	homozygous	139503164
14	32060784	32060785	C	T	39	GENIC	possibly homozygous	139503165