chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	183154534	183154535	C	T	15	GENIC	homozygous	136403994
2	183155266	183155266		AA	8	GENIC	homozygous	135965825
2	183155349	183155350	C	T	15	GENIC	homozygous	136403995
2	183155556	183155557	G	A	11	GENIC	homozygous	136403996
2	183155959	183155960	T	C	10	GENIC	homozygous	136403997
2	183158430	183158431	A	G	16	GENIC	homozygous	136403998
2	183159210	183159211	A	G	15	GENIC	homozygous	136403999
2	183159657	183159657		T	10	GENIC	homozygous	135965826
2	183160042	183160043	A		11	GENIC	homozygous	135965827
2	183160845	183160846	A	T	12	GENIC	homozygous	136404000
2	183161006	183161007	C	T	12	GENIC	homozygous	136404001
2	183161347	183161347		G	9	GENIC	homozygous	135965828
2	183163385	183163386	C	T	11	GENIC	homozygous	136404002
2	183163954	183163955	G	A	11	GENIC	homozygous	136404003
2	183166035	183166036	C	T	14	GENIC	homozygous	136404004
2	183167003	183167004	T	C	14	GENIC	homozygous	136404005
2	183169460	183169461	C	T	17	GENIC	homozygous	136404006
2	183171260	183171261	A	G	11	GENIC	homozygous	136404007
2	183173561	183173561		TT	8	GENIC	homozygous	135965829
2	183174880	183174881	G		5	GENIC	homozygous	135965830
2	183174881	183174882	G	A	5	GENIC	homozygous	136404008
2	183177502	183177503	T	A	18	GENIC	homozygous	136404009
2	183178579	183178580	G	A	16	GENIC	homozygous	136404010