chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50373743	50373744	A	C	9	GENIC	homozygous	114340139
13	50373919	50373920	T	C	12	GENIC	homozygous	114340143
13	50374227	50374228	G	A	5	GENIC	homozygous	114340144
13	50374577	50374578	G	A	10	GENIC	homozygous	114340146
13	50374625	50374626	C	T	14	GENIC	homozygous	114340148
13	50374861	50374862	T	C	13	GENIC	homozygous	114340150
13	50375047	50375048	A	C	9	GENIC	homozygous	114340151
13	50375095	50375096	A	G	14	GENIC	homozygous	114340153
13	50375161	50375162	T	C	13	GENIC	homozygous	114340155
13	50375355	50375356	T	A	11	GENIC	homozygous	114549940
13	50375642	50375643	A	G	9	GENIC	homozygous	114340157
13	50375650	50375651	G	A	10	GENIC	homozygous	114340159
13	50375690	50375691	C	T	6	GENIC	homozygous	114340161
13	50375736	50375737	A	G	8	GENIC	homozygous	114340163
13	50376319	50376320	A	G	9	GENIC	homozygous	114340165
13	50376346	50376347	A	G	5	GENIC	homozygous	114340167
13	50376962	50376963	A	G	15	GENIC	homozygous	114340169
13	50377227	50377228	C	T	6	GENIC	homozygous	114340173
13	50377290	50377291	T	C	14	GENIC	homozygous	114340175
13	50377637	50377638	T	G	14	GENIC	homozygous	114340177
13	50377787	50377788	A	G	7	GENIC	homozygous	114340179
13	50378194	50378195	T	C	10	GENIC	homozygous	114340180
13	50378334	50378335	G	T	13	GENIC	possibly homozygous	114340182
13	50378535	50378536	G	A	9	GENIC	homozygous	114340184
13	50378627	50378628	G	A	8	GENIC	homozygous	114340186
13	50378816	50378817	G	T	8	GENIC	homozygous	114340188
13	50378904	50378905	T	G	7	GENIC	homozygous	114340190
13	50378924	50378925	A	G	9	GENIC	homozygous	114340192
13	50379233	50379234	A	G	6	GENIC	homozygous	114340196
13	50379397	50379398	T	C	9	GENIC	homozygous	114340198
13	50379427	50379428	T	G	12	GENIC	homozygous	114340199
13	50379438	50379439	T	G	12	GENIC	homozygous	114340201
13	50379484	50379485	A	G	13	GENIC	homozygous	114340203
13	50380464	50380465	T	C	15	GENIC	homozygous	114340205
13	50380751	50380752	G	T	12	GENIC	homozygous	114340207