chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	50726293	50726294	T	A	29	GENIC	possibly homozygous	114797910
6	50730882	50730883	T	A	30	GENIC	homozygous	114797911
6	50734353	50734354	C	T	31	GENIC	homozygous	114797920
6	50734394	50734395	T	C	35	GENIC	homozygous	114797921
6	50736549	50736550	C	T	22	GENIC	homozygous	114797922
6	50738930	50738931	A	G	32	GENIC	homozygous	114797923
6	50742305	50742306	A	G	25	GENIC	homozygous	114797925
6	50742560	50742561	A	C	20	GENIC	homozygous	114797926
6	50743017	50743018	A	G	26	GENIC	homozygous	114797927
6	50743696	50743697	G	A	24	GENIC	homozygous	114797929
6	50744122	50744123	A	C	21	GENIC	homozygous	114797930
6	50746305	50746306	G	T	21	GENIC	homozygous	114797932
6	50746319	50746320	C	G	25	GENIC	homozygous	114797933
6	50746362	50746363	T	C	37	GENIC	homozygous	114797934
6	50746634	50746635	C	T	48	GENIC	homozygous	114797935
6	50746740	50746741	T	C	29	GENIC	homozygous	114797936
6	50746757	50746758	A	G	32	GENIC	homozygous	114797937
6	50747640	50747641	G	A	15	GENIC	homozygous	114797938
6	50747759	50747760	T	G	33	GENIC	homozygous	114797939
6	50747827	50747828	A	G	23	GENIC	homozygous	114797940
6	50748281	50748282	A	G	12	GENIC	homozygous	114797941
6	50748792	50748793	T	C	21	GENIC	homozygous	114797942
6	50752127	50752128	T	C	35	GENIC	homozygous	114797943
6	50754950	50754951	C	T	13	GENIC	homozygous	114797944
6	50755755	50755756	G	A	27	GENIC	homozygous	114797945
6	50757314	50757315	T	A	16	GENIC	homozygous	114797949
6	50757352	50757353	T	A	19	GENIC	homozygous	114797950
6	50758415	50758416	C	T	21	GENIC	homozygous	114797951
6	50758597	50758598	A	G	34	GENIC	homozygous	114797952
6	50758608	50758609	C	T	28	GENIC	homozygous	114797953
6	50762797	50762798	G	T	24	GENIC	homozygous	114797954
6	50764559	50764560	A	G	35	GENIC	homozygous	114797955
6	50764810	50764811	T	C	27	GENIC	homozygous	114797956
6	50765779	50765780	C	A	38	GENIC	homozygous	114797957