chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	104477431	104477432	G	T	19	GENIC	homozygous	108905181
1	104477450	104477451	G	A	24	GENIC	homozygous	109423003
1	104477451	104477452	A	C	23	GENIC	homozygous	109119606
1	104478304	104478305	C	T	32	GENIC	possibly homozygous	108905182
1	104478470	104478471	G	A	34	GENIC	homozygous	109423007
1	104478570	104478571	G	A	26	GENIC	homozygous	108905183
1	104478785	104478786	A	G	22	GENIC	homozygous	108905184
1	104478921	104478922	T	C	31	GENIC	homozygous	108905185
1	104479048	104479049	G	C	32	GENIC	homozygous	108905186
1	104479079	104479080	G	A	28	GENIC	homozygous	108905187
1	104479358	104479359	T	C	27	GENIC	homozygous	108905188
1	104480826	104480827	A	C	30	GENIC	homozygous	108905189
1	104480929	104480930	A	G	32	GENIC	homozygous	108905190
1	104481234	104481235	A	G	34	GENIC	homozygous	108905191