chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	71211417	71211418	T	A	23	GENIC	homozygous	111606386
3	71213905	71213906	A	T	14	GENIC	homozygous	111606387
3	71215425	71215426	A	G	28	GENIC	homozygous	111606388
3	71218674	71218675	G	A	26	GENIC	homozygous	111606389
3	71219444	71219445	C	T	40	GENIC	homozygous	111606390
3	71219518	71219519	G	A	33	GENIC	homozygous	111606391
3	71219636	71219637	C	T	29	GENIC	homozygous	111606392
3	71219843	71219844	G	A	45	GENIC	homozygous	111606393
3	71221098	71221099	G	T	38	GENIC	homozygous	111606395
3	71221777	71221778	T	A	34	GENIC	homozygous	111606396
3	71222109	71222110	A	G	43	GENIC	homozygous	111606397
3	71223395	71223396	C	T	32	GENIC	homozygous	111606399
3	71223562	71223563	A	T	25	GENIC	homozygous	111606400
3	71225058	71225059	C	T	24	GENIC	homozygous	119649967
3	71244852	71244853	G	A	29	GENIC	homozygous	111606401
3	71247137	71247138	G	A	46	GENIC	homozygous	111606402