chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97213984	97213984		T	16	GENIC	homozygous	128850066
10	97215977	97215977		AAT	11	GENIC	homozygous	128850067
10	97222652	97222652		TG	20	GENIC	homozygous	128850068
10	97223298	97223299	C	T	22	GENIC	homozygous	116693177
10	97223109	97223110	T	C	16	GENIC	homozygous	116693175
10	97221691	97221692	G		3	GENIC	homozygous	129970594
10	97221699	97221700	A	T	2	GENIC	homozygous	129974016
10	97221700	97221701	G	A	2	GENIC	homozygous	129974017
10	97226173	97226174	A	T	13	GENIC	homozygous	118076166
10	97229907	97229908	G	A	7	GENIC	homozygous	116693179
10	97230708	97230709	A	G	17	GENIC	homozygous	116693181
10	97231607	97231608	G		15	GENIC	homozygous	128850069
10	97231670	97231671	T	C	18	GENIC	homozygous	116693183
10	97232911	97232912	C	T	11	GENIC	homozygous	116693185
10	97233294	97233310	GTGTGTGTGTAATGCC		8	GENIC	homozygous	128850070
10	97233889	97233890	G	A	25	GENIC	homozygous	116693187
10	97236529	97236530	C	G	15	GENIC	homozygous	116693189
10	97237417	97237418	T	C	28	GENIC	homozygous	116693191
10	97238230	97238242	CCGCGTGCACCT		18	GENIC	homozygous	128850071
10	97226163	97226164	A	T	15	GENIC	homozygous	128874198
10	97216014	97216015	C	G	14	GENIC	homozygous	116693171
10	97216410	97216411	A	G	13	GENIC	homozygous	116693173
10	97226169	97226170	A	T	14	GENIC	homozygous	118126147
10	97226171	97226172	A	T	13	GENIC	homozygous	118126148
10	97233274	97233275	G	A	7	GENIC	homozygous	118010214