chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97213481	97213482	T	G	21	GENIC	homozygous	116983089
10	97216410	97216411	A	G	23	GENIC	homozygous	116693173
10	97221709	97221710	G	T	3	GENIC	homozygous	118076164
10	97221710	97221711	A	T	3	GENIC	homozygous	118076165
10	97224474	97224475	C	T	27	GENIC	homozygous	116956254
10	97218710	97218711	C	T	27	GENIC	homozygous	116956248
10	97220505	97220506	C	T	37	GENIC	homozygous	116956250
10	97221013	97221014	A	G	33	GENIC	homozygous	116956252
10	97225419	97225420	C	T	35	GENIC	homozygous	116956256
10	97226173	97226174	A	T	11	GENIC	heterozygous	118076166
10	97230708	97230709	A	G	28	GENIC	homozygous	116693181
10	97231670	97231671	T	C	33	GENIC	homozygous	116693183
10	97234062	97234063	G	T	26	GENIC	homozygous	116956258
10	97234089	97234090	T	C	21	GENIC	homozygous	116956260
10	97235321	97235322	T	C	33	GENIC	homozygous	116956262
10	97235326	97235327	T	C	29	GENIC	homozygous	116956264
10	97236523	97236524	T	G	32	GENIC	homozygous	116956266
10	97236529	97236530	C	G	31	GENIC	homozygous	116693189
10	97236933	97236934	C	G	36	GENIC	homozygous	116956268
10	97237417	97237418	T	C	40	GENIC	homozygous	116693191
10	97233226	97233227	G	A	41	GENIC	homozygous	118070076
10	97228031	97228032	T	C	43	GENIC	homozygous	118010211
10	97228553	97228554	T	C	30	GENIC	homozygous	118010212
10	97229228	97229229	T	C	25	GENIC	homozygous	118010213