chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	49853819	49853820	A	G	38	GENIC	homozygous	117522813
9	49854689	49854690	T	C	34	GENIC	homozygous	117522817
9	49857575	49857576	T	C	37	GENIC	homozygous	117522821
9	49858825	49858826	G	A	24	GENIC	homozygous	117522823
9	49862346	49862347	T	C	15	GENIC	homozygous	117522829
9	49871957	49871958	T	C	19	GENIC	homozygous	117522855
9	49873034	49873035	G	A	25	GENIC	homozygous	120268260
9	49873088	49873089	A	C	28	GENIC	homozygous	117522859
9	49873315	49873316	C	T	35	GENIC	heterozygous	117522863
9	49873927	49873928	T	C	15	GENIC	homozygous	117522871
9	49874995	49874996	A	G	27	GENIC	homozygous	117522873
9	49875327	49875328	G	A	29	GENIC	homozygous	120268261
9	49877315	49877316	G	A	37	GENIC	homozygous	120268262
9	49880658	49880659	A	T	21	GENIC	homozygous	120268263
9	49881080	49881081	A	G	18	GENIC	homozygous	117522887
9	49881745	49881746	A	G	29	GENIC	homozygous	117522889
9	49884348	49884349	T	C	16	GENIC	homozygous	117522899
9	49887082	49887083	A	T	20	GENIC	homozygous	117522905
9	49889030	49889031	A	G	21	GENIC	homozygous	117522909
9	49889050	49889051	A	G	20	GENIC	homozygous	117522911
9	49889598	49889599	T	C	16	GENIC	homozygous	117522913
9	49890524	49890525	G	A	14	GENIC	homozygous	120268264
9	49892183	49892184	C	A	37	GENIC	homozygous	120268265
9	49893586	49893587	C	T	21	GENIC	homozygous	117522925
9	49896679	49896680	T	C	11	GENIC	homozygous	117539710
9	49896687	49896688	G	C	10	GENIC	possibly homozygous	117539712
9	49897101	49897102	G	T	23	GENIC	homozygous	120268266
9	49897338	49897339	G	C	25	GENIC	homozygous	117522933
9	49897472	49897473	C	T	20	GENIC	homozygous	120268267
9	49897860	49897861	C	G	13	GENIC	homozygous	120268268
9	49900082	49900083	A	C	11	GENIC	homozygous	120268269
9	49902218	49902219	T	C	19	GENIC	homozygous	117522945
9	49902431	49902432	A	C	12	GENIC	homozygous	117522947
9	49902438	49902439	T	C	14	GENIC	homozygous	117522949