chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	159534821	159534822	C	T	17	GENIC	homozygous	114072842
5	159535008	159535009	C		28	GENIC	homozygous	128265342
5	159535145	159535146	G	A	28	GENIC	homozygous	114072843
5	159535206	159535207	G		20	GENIC	homozygous	128265343
5	159535343	159535350	GCCAGCT		24	GENIC	homozygous	128265344
5	159535456	159535457	T	C	35	GENIC	homozygous	114072844
5	159536078	159536079	T	A	24	GENIC	homozygous	114072845
5	159536100	159536101	G	A	22	GENIC	homozygous	114072846
5	159536581	159536582	T	A	29	GENIC	homozygous	114072847
5	159536844	159536845	T	C	21	GENIC	homozygous	114072848
5	159538052	159538053	G	A	23	GENIC	homozygous	114072849
5	159538420	159538421	G	A	28	GENIC	homozygous	114072850
5	159538443	159538444	T	G	26	GENIC	homozygous	114072851
5	159538476	159538477	T	C	32	GENIC	homozygous	114072852
5	159538742	159538743	A	G	26	GENIC	homozygous	114072853
5	159539404	159539405	T	C	32	GENIC	heterozygous	114452558
5	159537026	159537027	T	C	23	GENIC	heterozygous	132308392
5	159539316	159539317	C	T	35	GENIC	heterozygous	114452550
5	159539343	159539344	G	A	29	GENIC	heterozygous	114452552
5	159539368	159539369	C	T	30	GENIC	heterozygous	114452554
5	159539400	159539401	G	T	30	GENIC	heterozygous	114452556