chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	48529928	48529929	C	T	20	GENIC	homozygous	137768696
6	48531071	48531072	G	A	25	GENIC	homozygous	137768697
6	48531777	48531778	T	A	28	GENIC	homozygous	137768698
6	48532470	48532471	C	A	28	GENIC	homozygous	137768699
6	48532615	48532616	T	C	27	GENIC	homozygous	137768700
6	48533630	48533631	A		20	GENIC	possibly homozygous	403603860
6	48533633	48533634	A	T	20	GENIC	heterozygous	403603862
6	48532073	48532074	A	G	13	GENIC	homozygous	154359960
6	48533630	48533631	A	T	20	GENIC	heterozygous	154359962
6	48533633	48533634	A		20	GENIC	possibly homozygous	403603861
6	48533634	48533635	A	T	21	GENIC	heterozygous	154359963
6	48533634	48533635	A		21	GENIC	heterozygous	403603863
6	48538492	48538493	G	A	20	GENIC	homozygous	137768701
6	48539892	48539893	T	C	19	GENIC	homozygous	137768702
6	48541270	48541271	G	A	21	GENIC	homozygous	137768703
6	48542041	48542042	G	C	21	GENIC	homozygous	137768704
6	48543777	48543778	A	T	27	GENIC	homozygous	137768705
6	48543899	48543900	A	G	15	GENIC	homozygous	137768706
6	48545319	48545320	C	A	9	GENIC	homozygous	403603864
6	48545694	48545695	G	A	17	GENIC	homozygous	137768709
6	48534878	48534878		A	20	GENIC	homozygous	137680976
6	48543852	48543853	T		17	GENIC	homozygous	137680977
6	48545406	48545407	A	G	13	GENIC	homozygous	137768707
6	48545638	48545639	A	C	15	GENIC	homozygous	137768708
6	48547026	48547027	C	T	25	GENIC	homozygous	137768710
6	48547277	48547278	T	C	17	GENIC	homozygous	137768711
6	48547291	48547292	C	T	18	GENIC	homozygous	137768712
6	48548070	48548070		A	14	GENIC	possibly homozygous	137680978
6	48549155	48549156	G	A	28	GENIC	homozygous	137768713
6	48549608	48549609	T		11	GENIC	heterozygous	137680979
6	48549857	48549858	A	G	25	GENIC	homozygous	137768714
6	48552892	48552893	G	A	29	GENIC	homozygous	137768715
6	48553862	48553863	T	G	25	GENIC	homozygous	137768716
6	48551508	48551509	G		6	GENIC	homozygous	140887838