chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	91206699	91206700	A	T	40	GENIC	homozygous	111653557
3	91206710	91206711	T	A	41	GENIC	homozygous	111653558
3	91206981	91206982	C	T	58	GENIC	homozygous	119980121
3	91207352	91207353	C	A	51	GENIC	homozygous	119980122
3	91207761	91207762	C	T	58	GENIC	homozygous	119980123
3	91207854	91207855	A	G	74	GENIC	homozygous	111653560
3	91208211	91208212	G	A	39	GENIC	possibly homozygous	111653562
3	91208274	91208275	T	C	45	GENIC	homozygous	111653563
3	91208366	91208367	T	C	56	GENIC	homozygous	111653564
3	91208640	91208641	A	G	50	GENIC	homozygous	119980124
3	91209026	91209027	A	C	55	GENIC	homozygous	111653566
3	91209128	91209129	T	A	44	GENIC	homozygous	119980125
3	91209517	91209518	C	T	33	GENIC	homozygous	119980126
3	91209557	91209558	A	G	41	GENIC	homozygous	111653568
3	91209950	91209951	C	T	51	GENIC	homozygous	111653569
3	91210148	91210149	C	T	51	GENIC	homozygous	111653570
3	91210943	91210944	T	G	55	GENIC	homozygous	111653571
3	91211824	91211825	G	C	41	GENIC	homozygous	111653573
3	91213023	91213024	C	A	60	GENIC	homozygous	111653574
3	91213078	91213079	T	C	59	GENIC	homozygous	111653575
3	91213252	91213253	G	A	47	GENIC	homozygous	119980127
3	91213347	91213348	A	G	44	GENIC	homozygous	111653576
3	91213418	91213419	C	T	58	GENIC	homozygous	111653577
3	91214231	91214232	T	C	47	GENIC	homozygous	111653578
3	91214520	91214521	A	C	51	GENIC	homozygous	111653579
3	91214531	91214532	A	C	49	GENIC	homozygous	111653580
3	91215214	91215215	A	T	64	GENIC	possibly homozygous	119980128
3	91215339	91215340	G	A	49	GENIC	homozygous	111653581
3	91208142	91208143	A		43	GENIC	homozygous	131625909
3	91208952	91208952		A	52	GENIC	homozygous	131625910
3	91209621	91209621		G	39	GENIC	homozygous	127908459
3	91217088	91217092	GTTA		41	GENIC	homozygous	127908460