chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14678375	14678376	C	T	53	GENIC	homozygous	116737182
10	14678697	14678698	G	A	42	GENIC	homozygous	116737183
10	14679050	14679051	T	C	56	GENIC	homozygous	116737184
10	14679070	14679071	T	C	54	GENIC	homozygous	116737185
10	14679203	14679204	A	C	37	GENIC	homozygous	116496849
10	14679261	14679262	T	G	40	GENIC	homozygous	116737186
10	14679303	14679304	G	T	51	GENIC	homozygous	116737187
10	14679352	14679353	G	A	51	GENIC	homozygous	116737188
10	14679381	14679420	CCCATAAAACACCTGGGATACCTGGTACTTCTGAGACAC		56	GENIC	homozygous	131088063
10	14679566	14679567	C	T	48	GENIC	possibly homozygous	116737189
10	14679755	14679756	A	C	53	GENIC	homozygous	116496851
10	14679781	14679782	T	C	61	GENIC	homozygous	116859733
10	14679803	14679804	C	T	62	GENIC	homozygous	116859735
10	14679826	14679827	C	T	61	GENIC	homozygous	116859737
10	14679921	14679922	A	G	62	GENIC	homozygous	116737190
10	14679949	14679950	T	C	65	GENIC	homozygous	116737191
10	14679974	14679975	C	G	64	GENIC	homozygous	116737192
10	14679996	14679997	T	C	62	GENIC	homozygous	116737193
10	14680005	14680006	G	A	64	GENIC	homozygous	116737194
10	14680010	14680011	C	G	62	GENIC	homozygous	116496853
10	14680038	14680039	A	G	65	GENIC	homozygous	116737195
10	14680051	14680052	G	C	67	GENIC	homozygous	116737196
10	14680152	14680153	A	C	76	GENIC	homozygous	116859739
10	14680271	14680272	T	G	65	GENIC	possibly homozygous	116737197
10	14680328	14680328		G	51	GENIC	homozygous	131088064
10	14680336	14680336		CAGAAAGCCTGGAC	53	GENIC	homozygous	131088065
10	14680341	14680341		AAGGTTGTTCTAG	46	GENIC	homozygous	131088066
10	14680487	14680488	T	C	53	GENIC	homozygous	116737198
10	14680549	14680550	C		58	GENIC	homozygous	131088067
10	14681294	14681295	C	T	62	GENIC	homozygous	116737199
10	14681314	14681314		CTC	64	GENIC	homozygous	131088068
10	14681395	14681396	T	C	58	GENIC	homozygous	116496855
10	14681562	14681563	T	C	55	GENIC	homozygous	116496857
10	14681865	14681866	T	C	43	GENIC	homozygous	116496859