chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	32046833	32046834	A	T	29	GENIC	homozygous	139503149
14	32047447	32047448	C	T	33	GENIC	homozygous	139503150
14	32048147	32048148	T	C	17	GENIC	homozygous	139503151
14	32048515	32048516	G	A	46	GENIC	homozygous	139503152
14	32048648	32048649	T	C	32	GENIC	homozygous	139503153
14	32048956	32048957	C	T	45	GENIC	homozygous	139503154
14	32049492	32049493	G	A	38	GENIC	homozygous	139503155
14	32049624	32049625	T	G	48	GENIC	possibly homozygous	139503156
14	32050257	32050258	C	T	28	GENIC	homozygous	139503157
14	32052616	32052617	G	A	57	GENIC	homozygous	139503159
14	32048291	32048291		T	21	GENIC	homozygous	139390308
14	32050207	32050207		ACAGCC	20	GENIC	homozygous	139390309
14	32050258	32050259	T	G	28	GENIC	homozygous	139503158
14	32052699	32052700	A	G	40	GENIC	homozygous	139503160
14	32056318	32056322	TTCT		39	GENIC	possibly homozygous	139390310
14	32057291	32057291		AC	31	GENIC	homozygous	139390311
14	32058124	32058125	G	A	40	GENIC	homozygous	139503161
14	32058914	32058915	T	C	45	GENIC	homozygous	139503162
14	32059170	32059171	C	G	37	GENIC	homozygous	139503163
14	32059478	32059479	A	G	36	GENIC	homozygous	139503164
14	32060784	32060785	C	T	40	GENIC	homozygous	139503165
14	32060035	32060035		GC	12	GENIC	heterozygous	145827559