chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	3080399	3080400	G	A	2	GENIC		71695150
3	3087344	3087345	T	G	58	GENIC	heterozygous	71695157
3	3108994	3108995	C	A	34	GENIC	homozygous	71695218
3	3109084	3109085	G	A	20	GENIC	homozygous	71695221
3	3110802	3110803	A	G	50	GENIC	homozygous	72601089
3	3110800	3110801	T	G	50	GENIC	possibly homozygous	72601087
3	3109041	3109042	T	C	30	GENIC	homozygous	72305575
3	3110804	3110805	C	T	52	GENIC	homozygous	71695224
3	3110826	3110827	T	C	51	GENIC	homozygous	71695227
3	3119062	3119063	G	C	13	GENIC	heterozygous	71695248
3	3145784	3145785	T	G	65	GENIC	heterozygous	72305577
3	3146067	3146068	T	C	29	GENIC	heterozygous	71695308
3	3148495	3148496	C	A	32	GENIC	possibly homozygous	71695317
3	3148521	3148522	C	G	33	GENIC	homozygous	71695320
3	3148555	3148556	T	C	27	GENIC	homozygous	71695323
3	3148568	3148569	G	C	31	GENIC	homozygous	71695326
3	3148626	3148627	C	G	27	GENIC	homozygous	71695329
3	3148630	3148631	C	G	28	GENIC	homozygous	71695333
3	3148648	3148649	T	G	30	GENIC	homozygous	71695336
3	3148878	3148879	A	C	47	GENIC	homozygous	71695339
3	3168708	3168709	A	G	62	GENIC	heterozygous	71695375
3	3168712	3168713	G	A	62	GENIC	heterozygous	71695378