chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	104623432	104623433	C	T	27	GENIC	homozygous	114932133
6	104623805	104623806	A	G	34	GENIC	homozygous	114932134
6	104625829	104625830	A	T	16	GENIC	possibly homozygous	114932137
6	104626093	104626094	G	A	25	GENIC	homozygous	114932138
6	104626396	104626397	C	A	24	GENIC	possibly homozygous	114932139
6	104626444	104626445	G	A	25	GENIC	possibly homozygous	118733182
6	104626694	104626695	G	A	16	GENIC	possibly homozygous	118733183
6	104627153	104627154	G	T	27	GENIC	homozygous	114932142
6	104627181	104627182	T	G	32	GENIC	homozygous	114932143
6	104627514	104627515	G	C	30	GENIC	possibly homozygous	114932145
6	104627519	104627520	A	G	30	GENIC	possibly homozygous	114932146
6	104627558	104627559	C	T	22	GENIC	possibly homozygous	114932147
6	104627599	104627600	C	T	19	GENIC	possibly homozygous	118733184
6	104628005	104628006	C	T	29	GENIC	homozygous	118733185
6	104629531	104629532	C	G	30	GENIC	possibly homozygous	114932154
6	104629621	104629622	C	A	33	GENIC	possibly homozygous	118733186
6	104629720	104629721	G	A	26	GENIC	possibly homozygous	118733187
6	104629802	104629803	G	A	27	GENIC	homozygous	118733188