chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	148893125	148893128	TTT		25	GENIC	homozygous	136920754
4	148893448	148893449	C	T	22	GENIC	homozygous	137229927
4	148893823	148893824	A	G	19	GENIC	homozygous	137229928
4	148894332	148894333	T	C	13	GENIC	homozygous	137229929
4	148894767	148894770	CCT		9	GENIC	homozygous	136920755
4	148894798	148894799	A	G	11	GENIC	homozygous	137229930
4	148895135	148895136	C	T	18	GENIC	homozygous	137229931
4	148895257	148895258	A	C	10	GENIC	homozygous	137229932
4	148895378	148895379	T	C	13	GENIC	homozygous	137229933
4	148895493	148895494	G	A	20	GENIC	homozygous	137229934
4	148895686	148895687	C	T	25	GENIC	homozygous	137229935
4	148896500	148896501	T	C	18	GENIC	homozygous	137229936
4	148897627	148897628	G		20	GENIC	homozygous	136920756
4	148898198	148898199	A		14	GENIC	homozygous	136920757
4	148899111	148899112	C	G	17	GENIC	homozygous	137229941
4	148896673	148896674	T	C	12	GENIC	homozygous	137229937
4	148897884	148897885	T	C	26	GENIC	homozygous	137229938
4	148898019	148898020	A	G	26	GENIC	homozygous	137229939
4	148898232	148898233	A	G	13	GENIC	homozygous	137229940
4	148895569	148895570	T	C	19	GENIC	homozygous	143164646
4	148899597	148899601	AAGA		20	GENIC	homozygous	136920758
4	148900196	148900197	C	T	22	GENIC	homozygous	137229942
4	148901286	148901287	A	G	15	GENIC	homozygous	137229943
4	148902258	148902259	T	C	10	GENIC	homozygous	137229944
4	148902418	148902419	C	A	16	GENIC	homozygous	137229945
4	148903345	148903346	G	A	15	GENIC	homozygous	137229946
4	148904470	148904471	T	C	13	GENIC	homozygous	137229947