chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	104693147	104693148	A	C	13	GENIC	homozygous	117260739
10	104693434	104693435	T	G	18	GENIC	homozygous	116836141
10	104693589	104693590	T	C	13	GENIC	homozygous	116836143
10	104694176	104694177	C	T	17	GENIC	homozygous	116836147
10	104694350	104694351	A	G	10	GENIC	homozygous	116836149
10	104694668	104694669	A	G	21	GENIC	homozygous	116836151
10	104695009	104695010	C	T	16	GENIC	homozygous	116836153
10	104695548	104695549	G	A	11	GENIC	homozygous	116836155
10	104695859	104695860	A	G	16	GENIC	homozygous	116836157
10	104695878	104695879	T	G	18	GENIC	homozygous	116836159
10	104696435	104696436	C	G	7	GENIC	homozygous	117031178
10	104696772	104696773	A	G	11	GENIC	homozygous	116836161
10	104697186	104697187	G	A	14	GENIC	homozygous	116836163
10	104697604	104697605	T	C	9	GENIC	homozygous	117260741
10	104698368	104698369	C	T	11	GENIC	homozygous	116836167
10	104698532	104698533	T	C	6	GENIC	homozygous	116836169
10	104699099	104699100	A	C	15	GENIC	homozygous	116836171
10	104699819	104699820	T	G	14	GENIC	homozygous	116836173
10	104704727	104704728	G	A	22	GENIC	homozygous	116836177
10	104706408	104706409	C	T	12	GENIC	homozygous	116836179
10	104706584	104706585	G	A	24	GENIC	homozygous	116836181
10	104706694	104706695	C	T	27	GENIC	homozygous	116836183
10	104706720	104706721	T	C	28	GENIC	homozygous	116836185
10	104707347	104707348	A	G	15	GENIC	homozygous	116836187
10	104708785	104708786	A	G	26	GENIC	homozygous	116836189
10	104709435	104709436	G	A	11	GENIC	homozygous	116836191
10	104710219	104710220	C	T	16	GENIC	homozygous	117031180
10	104711205	104711206	A	G	26	GENIC	homozygous	116836193
10	104712079	104712080	C	T	14	GENIC	homozygous	116836195
10	104713081	104713082	G	A	17	GENIC	homozygous	116836197
10	104713087	104713088	T	A	18	GENIC	homozygous	116836199
10	104713824	104713825	G	A	25	GENIC	homozygous	116836201
10	104716462	104716463	A	T	19	GENIC	homozygous	117031182