chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	137651649	137651650	A	G	29	GENIC	homozygous	73078167
3	137651922	137651923	T	C	32	GENIC	homozygous	73078169
3	137652614	137652615	T	A	47	GENIC	homozygous	73078171
3	137652917	137652918	C	T	32	GENIC	homozygous	73078174
3	137653007	137653008	C	A	31	GENIC	homozygous	73078176
3	137653027	137653028	C	T	33	GENIC	homozygous	73078179
3	137653052	137653053	T	C	33	GENIC	homozygous	73078181
3	137653185	137653186	T	C	39	GENIC	homozygous	73078183
3	137653248	137653249	A	G	24	GENIC	homozygous	73078186
3	137653550	137653551	A	G	18	GENIC	homozygous	72500697
3	137653599	137653600	T	G	36	GENIC	homozygous	73078188
3	137653646	137653647	C	T	33	GENIC	homozygous	73078191
3	137653763	137653764	T	C	39	GENIC	homozygous	73078193
3	137653874	137653875	T	A	37	GENIC	homozygous	73078195
3	137653934	137653935	G	A	41	GENIC	homozygous	73078198
3	137654337	137654338	T	C	27	GENIC	homozygous	72500699
3	137654389	137654390	G	A	32	GENIC	homozygous	73078200
3	137654437	137654438	G	T	27	GENIC	homozygous	73078203