chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	261193360	261193361	T	C	28	GENIC	homozygous	108629170
1	261193591	261193592	C	G	30	GENIC	homozygous	108629171
1	261193710	261193711	C	T	33	GENIC	homozygous	108629172
1	261196631	261196632	C	G	31	GENIC	homozygous	108629174
1	261201046	261201047	G	A	28	GENIC	homozygous	108629178
1	261202462	261202463	C	T	28	GENIC	homozygous	108629179
1	261202491	261202492	C	T	28	GENIC	homozygous	108629180
1	261202973	261202974	A	G	12	GENIC	homozygous	108629184
1	261203906	261203907	A	C	26	GENIC	homozygous	108629185
1	261205342	261205343	A	G	23	GENIC	homozygous	108629186
1	261206167	261206168	T	C	29	GENIC	homozygous	108629187
1	261206346	261206347	T	C	35	GENIC	homozygous	108629188
1	261207793	261207794	T	G	17	GENIC	homozygous	108629189
1	261210684	261210685	C	G	32	GENIC	homozygous	108629190
1	261211562	261211563	T	C	30	GENIC	homozygous	108629191
1	261211607	261211608	C	T	28	GENIC	homozygous	108629192
1	261212295	261212296	C	T	29	GENIC	homozygous	108629193
1	261214087	261214088	G	A	27	GENIC	homozygous	108629194
1	261219019	261219020	C	G	22	GENIC	homozygous	108629195
1	261222612	261222613	T	C	26	GENIC	homozygous	108629197
1	261225486	261225487	T	C	18	GENIC	homozygous	108629198