chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	199163623	199163624	C	T	32	GENIC	possibly homozygous	110202152
2	199164516	199164517	T	C	19	GENIC	homozygous	110202153
2	199164911	199164912	T	C	20	GENIC	possibly homozygous	110202154
2	199166055	199166056	G	A	38	GENIC	homozygous	110202155
2	199166258	199166259	C	T	29	GENIC	possibly homozygous	110202156
2	199167338	199167339	C	A	33	GENIC	homozygous	110202157
2	199168169	199168170	C	T	32	GENIC	homozygous	110202158
2	199168570	199168571	G	A	26	GENIC	homozygous	110202159
2	199168615	199168616	A	G	29	GENIC	homozygous	110202160
2	199168639	199168640	C	T	29	GENIC	homozygous	110202161
2	199169305	199169306	T	C	29	GENIC	homozygous	110202162
2	199170223	199170224	A	C	21	GENIC	homozygous	110202163
2	199172327	199172328	G	A	34	GENIC	homozygous	111355639
2	199172411	199172412	C	A	31	GENIC	homozygous	120130106
2	199175629	199175630	T	C	17	GENIC	possibly homozygous	110202169
2	199176260	199176261	T	C	28	GENIC	homozygous	110202170
2	199176305	199176306	T	C	30	GENIC	possibly homozygous	110202171
2	199179067	199179068	G	A	27	GENIC	homozygous	110202174
2	199179478	199179479	T	C	30	GENIC	homozygous	110202175
2	199181839	199181840	T	C	22	GENIC	homozygous	110202177
2	199181885	199181886	A	G	29	GENIC	homozygous	110202178
2	199184110	199184111	G	A	29	GENIC	possibly homozygous	110202179