chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	51013722	51013723	T	C	39	GENIC	possibly homozygous	111565534
3	51014182	51014183	G	A	24	GENIC	homozygous	111565535
3	51014954	51014955	A	T	9	GENIC	homozygous	111565536
3	51015711	51015712	A	G	30	GENIC	possibly homozygous	111565537
3	51016579	51016580	A	T	43	GENIC	homozygous	111565538
3	51017167	51017168	C	T	21	GENIC	homozygous	112119912
3	51015770	51015771	C	T	28	GENIC	possibly homozygous	112276159
3	51017029	51017030	C	A	16	GENIC	homozygous	112276161
3	51017929	51017930	C	T	25	GENIC	homozygous	112276163
3	51018126	51018127	T	A	17	GENIC	homozygous	119700825