chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	11425172	11425172		TG	29	GENIC	homozygous	130900637
3	11425701	11425701		CACACACACACACACACACACACACTCACACACT	12	GENIC	homozygous	132820850
3	11425749	11425750	T	C	16	GENIC	homozygous	111446954
3	11426556	11426557	A		7	GENIC	homozygous	131325446
3	11426946	11427041	GCTCAGCCTGCCTTCTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGC		11	GENIC	homozygous	130900640
3	11427432	11427433	T	C	20	GENIC	homozygous	111446958
3	11431190	11431191	T	C	13	GENIC	homozygous	111446968
3	11430477	11430477		T	2	GENIC	homozygous	133813367
3	11428549	11428550	T	C	21	GENIC	homozygous	119771935
3	11430662	11430663	G	A	22	GENIC	homozygous	119771937
3	11431185	11431186	T	C	13	GENIC	homozygous	119771939
3	11431242	11431243	G	T	11	GENIC	homozygous	119771941