chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103303817	103303818	G	T	28	GENIC	homozygous	108165380
1	103303822	103303823	A	T	30	GENIC	homozygous	108165381
1	103303824	103303825	A	T	30	GENIC	homozygous	108165382
1	103303836	103303837	G	A	34	GENIC	homozygous	108165383
1	103303877	103303877		C	35	GENIC	homozygous	127409081
1	103305053	103305065	GCAATTGGCCCA		15	GENIC	heterozygous	127409082
1	103311719	103311720	A	T	26	GENIC	homozygous	108165384
1	103311722	103311723	A	G	26	GENIC	homozygous	108165385
1	103311724	103311725	C	G	26	GENIC	homozygous	108165386
1	103305066	103305067	C	T	11	GENIC	heterozygous	127546142
1	103305067	103305068	A	T	12	GENIC	heterozygous	131790662
1	103305079	103305080	C	T	14	GENIC	heterozygous	131790663
1	103305090	103305091	G	A	12	GENIC	heterozygous	131790664
1	103305071	103305075	GGCC		13	GENIC	heterozygous	131779383