chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103747075	103747076	T	A	37	GENIC	homozygous	109509267
1	103747762	103747763	A	G	22	GENIC	homozygous	108903870
1	103749359	103749360	T	C	28	GENIC	homozygous	108903872
1	103751167	103751168	G	A	17	GENIC	homozygous	108903874
1	103752080	103752081	C	T	29	GENIC	homozygous	109117545
1	103752377	103752378	T	A	32	GENIC	homozygous	109117547
1	103753282	103753283	C	T	15	GENIC	homozygous	109117549
1	103753359	103753360	G	A	14	GENIC	homozygous	108903878
1	103753448	103753449	A	G	29	GENIC	homozygous	108903879
1	103753602	103753603	T	A	21	GENIC	homozygous	108903880
1	103753992	103753993	T	C	15	GENIC	homozygous	108903881
1	103755003	103755004	T	C	24	GENIC	homozygous	108903883
1	103755935	103755936	C	T	21	GENIC	homozygous	109117551
1	103756468	103756469	G	A	24	GENIC	homozygous	109117553
1	103756858	103756859	G	C	17	GENIC	homozygous	108903890
1	103757758	103757759	T	C	17	GENIC	homozygous	108903891
1	103757814	103757815	T	C	14	GENIC	homozygous	108903893
1	103758268	103758269	C	T	34	GENIC	homozygous	109117555
1	103759092	103759093	T	A	23	GENIC	homozygous	108903895
1	103759145	103759146	A	G	28	GENIC	homozygous	108903896
1	103759748	103759749	A	G	26	GENIC	homozygous	109117557
1	103760299	103760300	T	C	31	GENIC	homozygous	109117559
1	103760484	103760485	T	C	19	GENIC	homozygous	109117561