chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	103968884	103968885	T	C	20	GENIC	homozygous	111663345
3	103971274	103971275	G	A	30	GENIC	homozygous	111663354
3	103971876	103971877	G	A	26	GENIC	homozygous	111663356
3	103975750	103975751	C	A	33	GENIC	homozygous	111990985
3	103975822	103975823	G	A	32	GENIC	homozygous	111663368
3	103984673	103984674	T	C	28	GENIC	homozygous	111990989
3	103984739	103984740	T	A	27	GENIC	homozygous	111990991
3	103995264	103995265	T	A	21	GENIC	homozygous	111663413
3	104000296	104000297	C	T	30	GENIC	homozygous	111990999
3	104001878	104001879	A	C	19	GENIC	homozygous	111991001
3	104002516	104002517	A	G	32	GENIC	homozygous	111663435
3	104003698	104003699	C	G	31	GENIC	homozygous	111991003
3	104005506	104005507	T	C	32	GENIC	homozygous	111991005
3	104007328	104007329	T	A	32	GENIC	homozygous	111991015
3	104007469	104007470	C	G	34	GENIC	homozygous	111991017
3	104007645	104007646	T	C	10	GENIC	heterozygous	111663450
3	104014595	104014596	A	G	26	GENIC	homozygous	111663457
3	104014773	104014774	T	G	37	GENIC	homozygous	111991019
3	104015396	104015397	G	A	31	GENIC	homozygous	111991021
3	104015427	104015428	A	T	28	GENIC	homozygous	111991023
3	104015467	104015468	G	T	22	GENIC	homozygous	111663460
3	104015603	104015604	T	C	21	GENIC	homozygous	111991025
3	104015678	104015679	T	G	25	GENIC	homozygous	111991027
3	104015971	104015972	G	A	23	GENIC	homozygous	111991029
3	104018053	104018054	C	T	14	GENIC	homozygous	111991031