chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	12021137	12021138	C	T	29	GENIC	homozygous	111448769
3	12021195	12021196	G	A	30	GENIC	homozygous	112331313
3	12021285	12021286	A	G	23	GENIC	homozygous	111448773
3	12021300	12021301	T	C	23	GENIC	homozygous	111448775
3	12024999	12025000	C	T	25	GENIC	homozygous	111448805
3	12025144	12025145	T	A	17	GENIC	homozygous	111448809
3	12025636	12025637	C	T	28	GENIC	homozygous	111448815
3	12025943	12025944	A	G	23	GENIC	homozygous	112331316
3	12026004	12026005	G	A	22	GENIC	homozygous	112331318
3	12026058	12026059	C	A	22	GENIC	homozygous	112331321
3	12026449	12026449		AA	15	GENIC	homozygous	132038514
3	12026344	12026356	GTGAAGCCGTCA		13	GENIC	homozygous	132038512
3	12026448	12026448		AA	14	GENIC	homozygous	132038513
3	12026450	12026450		AA	15	GENIC	homozygous	132038515
3	12026451	12026453	GG		16	GENIC	homozygous	132038516
3	12026520	12026521	A	G	20	GENIC	homozygous	111448819
3	12026580	12026581	C	T	26	GENIC	homozygous	112331323
3	12027648	12027649	T	G	25	GENIC	homozygous	111448823
3	12028494	12028495	G	A	17	GENIC	homozygous	111448825
3	12027491	12027492	T	C	11	GENIC	heterozygous	132045913
3	12027492	12027493	T	C	10	GENIC	heterozygous	132289840