chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	133406600	133406601	T	C	21	GENIC	homozygous	112832599
4	133406762	133406763	C	T	17	GENIC	homozygous	112832601
4	133406818	133406819	A	G	15	GENIC	homozygous	112832602
4	133407260	133407261	A	G	27	GENIC	homozygous	112832603
4	133407364	133407365	C	T	19	GENIC	homozygous	113385282
4	133407539	133407540	C	T	20	GENIC	homozygous	112832604
4	133407541	133407542	C	T	21	GENIC	homozygous	112832605
4	133408381	133408382	A	G	23	GENIC	homozygous	112832607
4	133408819	133408820	T	C	25	GENIC	homozygous	112832608
4	133408859	133408860	C	A	26	GENIC	homozygous	112832609
4	133410072	133410073	G	A	11	GENIC	homozygous	113385284
4	133410597	133410598	C	T	28	GENIC	homozygous	112832612
4	133411368	133411369	G	A	29	GENIC	homozygous	112832613
4	133411563	133411564	A	G	18	GENIC	homozygous	113306506
4	133411657	133411658	A	G	28	GENIC	homozygous	113306507
4	133412310	133412311	C	T	14	GENIC	homozygous	113306508
4	133412869	133412870	C	T	22	GENIC	homozygous	113306511
4	133412978	133412979	T	G	26	GENIC	homozygous	112832617
4	133413098	133413099	G	A	22	GENIC	homozygous	113306512