chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	21181121	21181122	C	T	38	GENIC	homozygous	112108169
16	21181712	21181713	C	T	20	GENIC	homozygous	112108171
16	21196315	21196316	T	A	21	GENIC	homozygous	111754099
16	21198018	21198019	T	C	34	GENIC	homozygous	112108173
16	21206875	21206876	C	T	19	GENIC	homozygous	112108175
16	21207020	21207021	A	G	32	GENIC	homozygous	111754127
16	21216415	21216416	C	G	20	GENIC	homozygous	111754151
16	21218193	21218194	T	C	31	GENIC	homozygous	111754157
16	21188017	21188018	A	G	25	GENIC	homozygous	119192825
16	21212678	21212679	G	C	12	GENIC	heterozygous	119216376
16	21201424	21201425	C	G	22	GENIC	homozygous	111949282
16	21222535	21222536	G	A	34	GENIC	homozygous	111949286
16	21226673	21226674	A	G	23	GENIC	homozygous	111754186
16	21228738	21228739	C	T	35	GENIC	possibly homozygous	112348772
16	21232861	21232862	T	C	28	GENIC	homozygous	111754204
16	21237357	21237358	G	T	25	GENIC	homozygous	112108177
16	21247217	21247218	G	A	29	GENIC	homozygous	112108179
16	21255138	21255139	T	C	28	GENIC	homozygous	111754292
16	21258888	21258889	C	T	28	GENIC	homozygous	111949296