chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103378471	103378472	T	C	27	GENIC	homozygous	108903284
1	103378481	103378482	C	T	27	GENIC	homozygous	108903285
1	103378487	103378488	T	C	28	GENIC	homozygous	108903286
1	103378502	103378503	A	G	26	GENIC	homozygous	108903287
1	103378519	103378520	C	T	31	GENIC	homozygous	108903288
1	103378596	103378597	T	C	24	GENIC	homozygous	108903290
1	103378620	103378621	T	C	18	GENIC	homozygous	108903291
1	103378638	103378639	G	A	26	GENIC	homozygous	108903292
1	103379285	103379286	G	A	23	GENIC	homozygous	108903293
1	103379978	103379979	T	A	21	GENIC	homozygous	108903294
1	103379983	103379984	G	A	22	GENIC	homozygous	108903295
1	103382657	103382658	A	C	24	GENIC	homozygous	108903297
1	103383877	103383878	A	C	26	GENIC	homozygous	108903298
1	103385562	103385563	C	T	31	GENIC	homozygous	108903300
1	103385572	103385573	G	A	27	GENIC	homozygous	108903301
1	103385614	103385615	G	A	31	GENIC	homozygous	108903302
1	103385615	103385616	G	A	32	GENIC	homozygous	109116899
1	103385677	103385678	G	A	33	GENIC	homozygous	108903303
1	103387169	103387170	T	C	31	GENIC	homozygous	108903305
1	103387515	103387516	A	C	27	GENIC	homozygous	108903306
1	103387711	103387712	C	T	21	GENIC	homozygous	109116901
1	103388064	103388065	G	A	30	GENIC	homozygous	108903307
1	103388081	103388082	T	C	30	GENIC	homozygous	108903308
1	103388101	103388102	G	A	27	GENIC	homozygous	108903309