chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	103876614	103876615	G		30	GENIC	homozygous	139414839
14	103876644	103876644		C	40	GENIC	homozygous	139414840
14	103876810	103876811	C		46	GENIC	homozygous	139414841
14	103877068	103877069	A		60	GENIC	homozygous	139414842
14	103879144	103879145	T		47	GENIC	homozygous	139414844
14	103879200	103879200		G	53	GENIC	homozygous	139414845
14	103879233	103879233		C	49	GENIC	homozygous	139414846
14	103883360	103883360		G	65	GENIC	homozygous	139414847
14	103883403	103883403		T	63	GENIC	homozygous	139414848
14	103885048	103885048		A	53	GENIC	homozygous	139414850
14	103885443	103885443		A	64	GENIC	homozygous	139414851
14	103885647	103885647		C	53	GENIC	homozygous	139414852
14	103886628	103886628		A	51	GENIC	homozygous	139414853
14	103892144	103892145	A		6	GENIC	heterozygous	403368566
14	103892144	103892145	A	G	6	GENIC	heterozygous	403368567
14	103892144	103892145	A	C	6	GENIC	heterozygous	403368568
14	103892214	103892215	G	C	15	GENIC	heterozygous	403368572
14	103892214	103892215	G		15	GENIC	heterozygous	403368573
14	103894958	103894959	T		33	GENIC	possibly homozygous	139414855
14	103896248	103896248		C	53	GENIC	homozygous	139414856
14	103896398	103896398		A	44	GENIC	homozygous	139414857
14	103898630	103898631	G		57	GENIC	homozygous	139414859
14	103904146	103904146		G	11	GENIC	homozygous	139414860
14	103904161	103904162	G		10	GENIC	homozygous	139414861
14	103986234	103986235	G		19	GENIC	heterozygous	404026213
14	103986234	103986235	G	A	19	GENIC	heterozygous	404026214
14	103996965	103996966	T		41	GENIC	possibly homozygous	139414924