chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103378471	103378472	T	C	11	GENIC	homozygous	108903284
1	103378481	103378482	C	T	11	GENIC	homozygous	108903285
1	103378487	103378488	T	C	12	GENIC	homozygous	108903286
1	103378502	103378503	A	G	10	GENIC	homozygous	108903287
1	103378519	103378520	C	T	10	GENIC	homozygous	108903288
1	103378596	103378597	T	C	16	GENIC	homozygous	108903290
1	103378620	103378621	T	C	18	GENIC	homozygous	108903291
1	103378638	103378639	G	A	16	GENIC	homozygous	108903292
1	103379285	103379286	G	A	18	GENIC	homozygous	108903293
1	103379978	103379979	T	A	13	GENIC	homozygous	108903294
1	103379983	103379984	G	A	14	GENIC	homozygous	108903295
1	103382357	103382358	C	T	17	GENIC	homozygous	109420337
1	103382657	103382658	A	C	9	GENIC	homozygous	108903297
1	103383877	103383878	A	C	6	GENIC	heterozygous	108903298
1	103384227	103384228	A	G	11	GENIC	homozygous	108903299
1	103385562	103385563	C	T	7	GENIC	homozygous	108903300
1	103385572	103385573	G	A	8	GENIC	homozygous	108903301
1	103385614	103385615	G	A	10	GENIC	homozygous	108903302
1	103385677	103385678	G	A	15	GENIC	homozygous	108903303