chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103200837	103200838	G	A	25	GENIC	homozygous	108903024
1	103204956	103204957	T	C	19	GENIC	homozygous	108165372
1	103208936	103208937	A	G	16	GENIC	homozygous	108903025
1	103210168	103210169	C	T	37	GENIC	homozygous	108903026
1	103217291	103217292	T	C	17	GENIC	homozygous	108903027
1	103219391	103219392	C	T	16	GENIC	homozygous	108903028
1	103220002	103220003	G	T	29	GENIC	homozygous	108903029
1	103222428	103222429	G	T	22	GENIC	homozygous	108903030
1	103226399	103226400	T	C	21	GENIC	homozygous	108903032
1	103230514	103230515	G	A	26	GENIC	homozygous	108903033
1	103231645	103231646	C	A	21	GENIC	homozygous	108903034
1	103231881	103231882	T	C	24	GENIC	homozygous	108903035
1	103232247	103232248	G	A	24	GENIC	homozygous	108903036
1	103232319	103232320	A	G	28	GENIC	homozygous	108903037
1	103232335	103232336	A	G	25	GENIC	homozygous	108903038
1	103232472	103232473	C	T	20	GENIC	homozygous	108903039
1	103232631	103232632	G	A	25	GENIC	homozygous	108903040
1	103232636	103232637	A	G	25	GENIC	homozygous	108903041
1	103232804	103232805	T	C	21	GENIC	homozygous	108903043
1	103233557	103233558	G	A	19	GENIC	homozygous	108903044
1	103233861	103233862	G	T	23	GENIC	homozygous	108903045
1	103236476	103236477	C	T	23	GENIC	homozygous	108903046
1	103236794	103236795	C	T	24	GENIC	homozygous	108903047
1	103237630	103237631	C	T	27	GENIC	homozygous	108903048
1	103238041	103238042	G	A	27	GENIC	homozygous	108903049
1	103238847	103238848	T	C	24	GENIC	homozygous	108903050
1	103238980	103238981	G	T	24	GENIC	homozygous	108903051
1	103239797	103239798	T	A	27	GENIC	homozygous	108903052
1	103241125	103241126	C	T	22	GENIC	homozygous	108903053
1	103242157	103242158	G	A	19	GENIC	homozygous	108903054
1	103251525	103251526	T	C	23	GENIC	homozygous	108903057