chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	104611710	104611711	T	C	21	GENIC	homozygous	114932127
6	104611718	104611719	C	G	18	GENIC	homozygous	114932128
6	104617304	104617305	T	A	19	GENIC	homozygous	114932131
6	104617307	104617308	T	G	22	GENIC	homozygous	114932132
6	104622098	104622099	T	C	24	GENIC	homozygous	115147456
6	104623432	104623433	C	T	28	GENIC	homozygous	114932133
6	104623805	104623806	A	G	18	GENIC	homozygous	114932134
6	104630213	104630214	G	A	32	GENIC	possibly homozygous	115147457
6	104632532	104632533	C	G	26	GENIC	homozygous	114932161
6	104633493	104633494	G	A	23	GENIC	homozygous	115147458
6	104633799	104633800	C	T	53	GENIC	homozygous	115147459
6	104633905	104633906	T	C	47	GENIC	homozygous	114932166
6	104635172	104635173	C	A	13	GENIC	homozygous	114932170
6	104636359	104636360	C	T	58	GENIC	heterozygous	114932171
6	104636950	104636951	C	T	14	GENIC	homozygous	114932172
6	104637182	104637183	T	A	20	GENIC	homozygous	115147460
6	104637230	104637231	A	G	18	GENIC	homozygous	114932173
6	104637913	104637914	G	A	20	GENIC	homozygous	115147461
6	104638146	104638147	A	C	13	GENIC	heterozygous	115412008
6	104638515	104638516	G	C	28	GENIC	homozygous	114932175
6	104639783	104639784	C	T	33	GENIC	homozygous	115147462