chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	11092086	11092087	A	T	37	GENIC	homozygous	113339738
14	11092301	11092302	C	T	38	GENIC	homozygous	113339740
14	11092654	11092655	T	C	51	GENIC	homozygous	113339742
14	11092668	11092669	C	T	53	GENIC	homozygous	113339744
14	11092693	11092694	A	T	55	GENIC	possibly homozygous	113339746
14	11092947	11092948	T	C	79	GENIC	homozygous	114041542
14	11092983	11092984	A	G	57	GENIC	possibly homozygous	118675895
14	11092991	11092992	A	G	46	GENIC	possibly homozygous	118675896
14	11093095	11093096	C	T	169	GENIC	heterozygous	118675897
14	11093113	11093114	A	G	166	GENIC	heterozygous	118675898
14	11093131	11093132	C	T	184	GENIC	heterozygous	118675899
14	11093149	11093150	G	A	136	GENIC	homozygous	118675900
14	11093156	11093157	G	C	110	GENIC	heterozygous	118675901
14	11093213	11093214	G	A	60	GENIC	homozygous	113339748
14	11093807	11093808	G	A	54	GENIC	homozygous	113574606
14	11093892	11093893	A	G	42	GENIC	homozygous	113339750
14	11094477	11094478	A	T	46	GENIC	homozygous	113339752
14	11094744	11094745	A	G	49	GENIC	homozygous	113339754
14	11096066	11096067	C	T	39	GENIC	homozygous	113339756
14	11096162	11096163	T	C	42	GENIC	homozygous	113339758
14	11096550	11096551	C	A	59	GENIC	homozygous	113339760
14	11096702	11096703	G	A	34	GENIC	homozygous	113339762
14	11096752	11096753	G	C	36	GENIC	homozygous	113339764