chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97213327	97213331	TATC		24	GENIC	homozygous	128850065
10	97213481	97213482	T	G	25	GENIC	homozygous	116983089
10	97213984	97213984		T	32	GENIC	homozygous	128850066
10	97215977	97215977		AAT	32	GENIC	homozygous	128850067
10	97222652	97222652		TG	34	GENIC	homozygous	128850068
10	97225419	97225420	C	T	33	GENIC	homozygous	116956256
10	97216410	97216411	A	G	37	GENIC	homozygous	116693173
10	97218710	97218711	C	T	39	GENIC	homozygous	116956248
10	97220505	97220506	C	T	21	GENIC	homozygous	116956250
10	97221013	97221014	A	G	32	GENIC	homozygous	116956252
10	97224474	97224475	C	T	34	GENIC	possibly homozygous	116956254
10	97220322	97220325	CCA		36	GENIC	homozygous	132694403
10	97224363	97224365	GT		42	GENIC	possibly homozygous	132694404
10	97226169	97226170	A	T	13	GENIC	possibly homozygous	118126147
10	97226171	97226172	A	T	13	GENIC	possibly homozygous	118126148
10	97226173	97226174	A	T	12	GENIC	homozygous	118076166
10	97230708	97230709	A	G	44	GENIC	homozygous	116693181
10	97231607	97231608	G		37	GENIC	homozygous	128850069
10	97231670	97231671	T	C	39	GENIC	homozygous	116693183
10	97236523	97236524	T	G	44	GENIC	homozygous	116956266
10	97233226	97233227	G	A	7	GENIC	homozygous	118070076
10	97234062	97234063	G	T	49	GENIC	homozygous	116956258
10	97234089	97234090	T	C	53	GENIC	homozygous	116956260
10	97235321	97235322	T	C	55	GENIC	homozygous	116956262
10	97235326	97235327	T	C	50	GENIC	homozygous	116956264
10	97236529	97236530	C	G	43	GENIC	homozygous	116693189
10	97236933	97236934	C	G	47	GENIC	homozygous	116956268
10	97237417	97237418	T	C	40	GENIC	homozygous	116693191
10	97238230	97238242	CCGCGTGCACCT		35	GENIC	homozygous	128850071
10	97237888	97237890	AG		42	GENIC	possibly homozygous	131469708