chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	104423873	104423874	A	G	54	GENIC	homozygous	137186374
4	104423928	104423929	G	C	52	GENIC	homozygous	137186375
4	104426042	104426043	T	C	77	GENIC	homozygous	137186376
4	104426636	104426637	G	A	57	GENIC	homozygous	137186377
4	104428805	104428806	T	C	50	GENIC	homozygous	137186378
4	104429285	104429286	T	A	31	GENIC	homozygous	137186379
4	104429289	104429290	T	A	35	GENIC	homozygous	137186380
4	104429977	104429978	G	A	78	GENIC	homozygous	137186381
4	104430572	104430573	G	A	50	GENIC	homozygous	137186382
4	104430998	104430999	G	C	50	GENIC	homozygous	137186383
4	104431804	104431805	G	T	54	GENIC	homozygous	137186384
4	104432110	104432111	G	A	47	GENIC	homozygous	137186385
4	104432317	104432318	A	T	60	GENIC	homozygous	137186386
4	104434705	104434706	A	G	68	GENIC	homozygous	137186387
4	104434743	104434744	T	C	68	GENIC	homozygous	137186388
4	104431071	104431072	T		36	GENIC	homozygous	136909097
4	104434746	104434746		A	69	GENIC	homozygous	136909099
4	104428550	104428550		C	27	GENIC	homozygous	136909095
4	104430776	104430777	C		45	GENIC	homozygous	136909096
4	104432900	104432900		TC	43	GENIC	heterozygous	136909098