chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	193892863	193892864	T	G	47	GENIC	homozygous	110183845
2	193893000	193893001	T	C	46	GENIC	homozygous	110183846
2	193893328	193893329	A	G	44	GENIC	homozygous	110183847
2	193893449	193893450	C	A	51	GENIC	homozygous	110183848
2	193893652	193893653	G	A	40	GENIC	homozygous	110183849
2	193894139	193894140	T	C	30	GENIC	homozygous	110183850
2	193894296	193894297	T	C	33	GENIC	homozygous	110183851
2	193894778	193894779	A	G	39	GENIC	homozygous	110183852
2	193894864	193894865	A	G	34	GENIC	homozygous	110183853
2	193894986	193894987	T	C	38	GENIC	homozygous	110183854
2	193895806	193895807	A	G	37	GENIC	homozygous	110183856
2	193895931	193895932	G	A	44	GENIC	homozygous	110183857
2	193896189	193896190	A	G	43	GENIC	homozygous	110183858
2	193895582	193895582		C	39	GENIC	homozygous	127721006
2	193893629	193893629		G	36	GENIC	homozygous	127721003
2	193894050	193894050		TCTTTCTT	25	GENIC	homozygous	127721004
2	193894960	193894961	A		36	GENIC	homozygous	127721005
2	193896653	193896654	C	T	43	GENIC	homozygous	110183859
2	193897031	193897032	C	T	38	GENIC	homozygous	110183860
2	193897173	193897174	C	T	33	GENIC	homozygous	110183861
2	193897380	193897381	T	C	52	GENIC	homozygous	110183862
2	193897626	193897627	T	A	46	GENIC	homozygous	110183863
2	193899775	193899776	C	G	31	GENIC	homozygous	110183864
2	193900300	193900301	A	G	50	GENIC	homozygous	110183865