chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	110007053	110007054	A	G	12	GENIC	homozygous	114444234
13	110007297	110007298	C	A	4	GENIC	homozygous	114726242
13	110008208	110008209	G	A	19	GENIC	homozygous	114701756
13	110011233	110011234	C	G	19	GENIC	homozygous	114701760
13	110011971	110011972	T	G	18	GENIC	homozygous	114701764
13	110011177	110011178	T	G	23	GENIC	homozygous	114835191
13	110011824	110011825	C	T	4	GENIC	heterozygous	114835193
13	110015054	110015055	T	C	31	GENIC	homozygous	114444244
13	110015523	110015524	C	T	30	GENIC	homozygous	114701766
13	110016005	110016006	C	T	25	GENIC	possibly homozygous	114701768
13	110017921	110017922	T	C	23	GENIC	homozygous	114444254
13	110019205	110019206	C	A	26	GENIC	homozygous	114701784
13	110019926	110019927	T	A	36	GENIC	homozygous	114444260
13	110020403	110020404	A	G	30	GENIC	homozygous	114444262
13	110023137	110023138	G	A	27	GENIC	possibly homozygous	114701786
13	110023592	110023593	T	C	23	GENIC	homozygous	114701788
13	110023612	110023613	G	A	21	GENIC	homozygous	114701790
13	110023837	110023838	A	G	21	GENIC	homozygous	114444268
13	110026071	110026072	T	C	35	GENIC	homozygous	114835195
13	110027979	110027980	C	T	30	GENIC	homozygous	114701792
13	110030832	110030833	C	T	25	GENIC	homozygous	114835197