chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103115838	103115840	TC		21	GENIC	homozygous	130818531
1	103120521	103120522	T		3	GENIC	homozygous	130619527
1	103124387	103124388	T	C	30	GENIC	homozygous	109115934
1	103117807	103117808	T	G	1	GENIC	homozygous	127546121
1	103118831	103118832	G	A	14	GENIC	homozygous	109115924
1	103121193	103121194	T	C	20	GENIC	homozygous	109115926
1	103122266	103122267	T	C	13	GENIC	homozygous	109115928
1	103122309	103122310	T	C	14	GENIC	homozygous	109115930
1	103122694	103122695	G	T	22	GENIC	homozygous	109115932
1	103124896	103124898	GC		7	GENIC	possibly homozygous	130818532
1	103125461	103125462	A	G	19	GENIC	homozygous	109115936
1	103126641	103126642	A	G	24	GENIC	homozygous	109115938
1	103126955	103126955		C	16	GENIC	homozygous	130818533
1	103127126	103127127	G	T	24	GENIC	homozygous	109115940
1	103127512	103127513	C	G	25	GENIC	homozygous	109115942
1	103127746	103127746		AATGGCTTTGCCC	16	GENIC	homozygous	130818534
1	103128208	103128217	AACAAAAAC		24	GENIC	homozygous	130818535
1	103128268	103128269	G		32	GENIC	homozygous	130818536