chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	3108994	3108995	C	A	19	GENIC	possibly homozygous	71695218
3	3109084	3109085	G	A	32	GENIC	homozygous	71695221
3	3110802	3110803	A	G	27	GENIC	homozygous	72601089
3	3110804	3110805	C	T	27	GENIC	homozygous	71695224
3	3110826	3110827	T	C	37	GENIC	homozygous	71695227
3	3148495	3148496	C	A	30	GENIC	homozygous	71695317
3	3148521	3148522	C	G	23	GENIC	homozygous	71695320
3	3148555	3148556	T	C	23	GENIC	homozygous	71695323
3	3148568	3148569	G	C	22	GENIC	homozygous	71695326
3	3148626	3148627	C	G	15	GENIC	homozygous	71695329
3	3148630	3148631	C	G	16	GENIC	homozygous	71695333
3	3148648	3148649	T	G	17	GENIC	homozygous	71695336
3	3148878	3148879	A	C	34	GENIC	homozygous	71695339
3	3168700	3168701	A	G	33	GENIC	heterozygous	71695369
3	3168708	3168709	A	G	33	GENIC	heterozygous	71695375
3	3169141	3169142	C	T	38	GENIC	heterozygous	74938332