chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97213481	97213482	T	G	19	GENIC	homozygous	116983089
10	97216410	97216411	A	G	23	GENIC	homozygous	116693173
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	97224474	97224475	C	T	26	GENIC	homozygous	116956254
10	97225419	97225420	C	T	35	GENIC	homozygous	116956256
10	97230708	97230709	A	G	28	GENIC	homozygous	116693181
10	97231670	97231671	T	C	32	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	30	GENIC	homozygous	116693189
10	97236933	97236934	C	G	36	GENIC	homozygous	116956268
10	97237417	97237418	T	C	40	GENIC	homozygous	116693191