chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	148893125	148893128	TTT		51	GENIC	homozygous	136920754
4	148893448	148893449	C	T	56	GENIC	homozygous	137229927
4	148893823	148893824	A	G	52	GENIC	homozygous	137229928
4	148894332	148894333	T	C	44	GENIC	homozygous	137229929
4	148894767	148894770	CCT		48	GENIC	possibly homozygous	136920755
4	148894798	148894799	A	G	49	GENIC	homozygous	137229930
4	148895135	148895136	C	T	80	GENIC	homozygous	137229931
4	148895257	148895258	A	C	73	GENIC	homozygous	137229932
4	148895378	148895379	T	C	68	GENIC	homozygous	137229933
4	148895493	148895494	G	A	50	GENIC	homozygous	137229934
4	148895686	148895687	C	T	59	GENIC	homozygous	137229935
4	148896500	148896501	T	C	59	GENIC	homozygous	137229936
4	148896673	148896674	T	C	54	GENIC	homozygous	137229937
4	148897627	148897628	G		71	GENIC	homozygous	136920756
4	148897884	148897885	T	C	79	GENIC	homozygous	137229938
4	148898019	148898020	A	G	54	GENIC	homozygous	137229939
4	148898198	148898199	A		69	GENIC	homozygous	136920757
4	148898232	148898233	A	G	74	GENIC	homozygous	137229940
4	148899111	148899112	C	G	52	GENIC	homozygous	137229941
4	148899597	148899601	AAGA		55	GENIC	homozygous	136920758
4	148900196	148900197	C	T	65	GENIC	homozygous	137229942
4	148901286	148901287	A	G	66	GENIC	possibly homozygous	137229943
4	148902258	148902259	T	C	70	GENIC	homozygous	137229944
4	148902418	148902419	C	A	70	GENIC	homozygous	137229945
4	148903345	148903346	G	A	48	GENIC	homozygous	137229946
4	148904470	148904471	T	C	61	GENIC	homozygous	137229947