chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	104023835	104023836	A	G	20	GENIC	homozygous	108904421
1	104023897	104023898	C	T	19	GENIC	homozygous	108904422
1	104024905	104024906	A	C	19	GENIC	homozygous	108904423
1	104025849	104025850	G	A	15	GENIC	homozygous	108904424
1	104025855	104025856	T	A	14	GENIC	homozygous	108904425
1	104032979	104032980	C	A	14	GENIC	homozygous	108904428
1	104034203	104034204	G	A	11	GENIC	homozygous	108904430
1	104037044	104037045	C	T	21	GENIC	homozygous	108904431
1	104038036	104038037	A	G	13	GENIC	homozygous	108904432
1	104038472	104038473	A	G	20	GENIC	homozygous	108904434
1	104038551	104038552	G	A	20	GENIC	homozygous	108904435
1	104039220	104039221	C	T	23	GENIC	homozygous	108904436
1	104039395	104039396	A	G	19	GENIC	homozygous	108904437
1	104039465	104039466	G	A	20	GENIC	homozygous	108904438
1	104039682	104039683	T	A	18	GENIC	homozygous	109118824
1	104039683	104039684	A	G	18	GENIC	homozygous	109118826
1	104040042	104040043	G	C	13	GENIC	homozygous	108904439
1	104040490	104040491	C	T	22	GENIC	homozygous	108904440
1	104047818	104047819	G	A	22	GENIC	homozygous	108904443
1	104047908	104047909	A	C	25	GENIC	homozygous	108904444
1	104047977	104047978	G	A	23	GENIC	homozygous	108904445
1	104048074	104048075	C	A	16	GENIC	homozygous	108904446
1	104048589	104048590	C	T	24	GENIC	homozygous	108904447
1	104049253	104049254	G	A	24	GENIC	homozygous	108904448