chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	103913788	103913789	A	G	12	GENIC	homozygous	114928339
6	103913839	103913840	T	C	18	GENIC	possibly homozygous	114928341
6	103913929	103913930	T	A	46	GENIC	heterozygous	115222573
6	103913945	103913946	C	T	53	GENIC	heterozygous	115222575
6	103913980	103913981	C	T	63	GENIC	heterozygous	115503965
6	103914352	103914353	T	G	28	GENIC	possibly homozygous	115273362
6	103914389	103914390	T	A	64	GENIC	homozygous	114928351
6	103914499	103914500	G	T	18	GENIC	homozygous	115273366
6	103914529	103914530	C	A	31	GENIC	homozygous	115146150
6	103914582	103914583	G	T	97	GENIC	heterozygous	115146151
6	103914587	103914588	C	T	102	GENIC	heterozygous	115146152
6	103914597	103914598	C	A	129	GENIC	heterozygous	114928357
6	103914621	103914622	C	T	152	GENIC	heterozygous	115146154
6	103914641	103914642	T	G	152	GENIC	heterozygous	115146155
6	103914647	103914648	C	A	148	GENIC	heterozygous	114928359
6	103914769	103914770	G	A	217	GENIC	heterozygous	115146157
6	103914777	103914778	T	C	218	GENIC	heterozygous	115146158
6	103914790	103914791	T	A	220	GENIC	heterozygous	115146159
6	103914804	103914805	A	C	211	GENIC	heterozygous	115146160
6	103914859	103914860	T	G	145	GENIC	heterozygous	115146161
6	103914890	103914891	C	T	80	GENIC	heterozygous	115222579
6	103914928	103914929	A	G	41	GENIC	heterozygous	115146162
6	103914946	103914947	T	A	31	GENIC	heterozygous	115222581
6	103914971	103914972	T	A	20	GENIC	heterozygous	115146163
6	103914986	103914987	A	C	14	GENIC	homozygous	114928367
6	103915048	103915049	A	G	39	GENIC	homozygous	115222583
6	103915052	103915053	G	A	40	GENIC	heterozygous	115273368
6	103915130	103915131	G	T	100	GENIC	heterozygous	115222585
6	103915153	103915154	A	G	84	GENIC	homozygous	114928369