chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	182116612	182116613	G	T	29	GENIC	homozygous	136403099
2	182118604	182118605	C	T	39	GENIC	homozygous	142969168
2	182118615	182118616	T	C	41	GENIC	homozygous	142969169
2	182118630	182118631	G	A	46	GENIC	homozygous	142969170
2	182119259	182119269	GGTGTGAACT		23	GENIC	homozygous	142901848
2	182119284	182119285	G		26	GENIC	homozygous	142901849
2	182119739	182119740	C	G	16	GENIC	homozygous	142969171
2	182120289	182120290	T	C	36	GENIC	homozygous	142969172
2	182120548	182120552	ATAG		34	GENIC	homozygous	142901850
2	182120767	182120767		TGTGAGGG	26	GENIC	homozygous	142901851
2	182121098	182121099	C	T	25	GENIC	homozygous	142969174
2	182122571	182122572	T	C	28	GENIC	homozygous	142969175
2	182123072	182123073	C	A	32	GENIC	homozygous	154050342
2	182123760	182123761	T	C	27	GENIC	homozygous	142969176
2	182123772	182123773	G	A	32	GENIC	homozygous	142969177
2	182123798	182123799	C	G	35	GENIC	homozygous	142969178
2	182123803	182123804	C	T	38	GENIC	homozygous	142969179
2	182123852	182123853	C	T	41	GENIC	homozygous	142969180
2	182124170	182124171	C	T	28	GENIC	homozygous	142969181
2	182124248	182124248		GTTTT	23	GENIC	homozygous	142901852
2	182124438	182124439	T	C	30	GENIC	homozygous	136403102
2	182125948	182125949	T	G	36	GENIC	homozygous	142969183
2	182126248	182126249	G	A	26	GENIC	possibly homozygous	154051372
2	182126980	182126981	T	C	32	GENIC	homozygous	136403103
2	182127102	182127103	A	C	42	GENIC	homozygous	142969184
2	182123072	182123073	C	T	32	GENIC	heterozygous	403883525
2	182126248	182126249	G		26	GENIC	heterozygous	403883526
2	182125462	182125462		CTGTGTGGTTGGCTTTGAACTCA	26	GENIC	homozygous	135965542
2	182126724	182126726	CT		27	GENIC	homozygous	135965543
2	182128160	182128161	T	C	35	GENIC	homozygous	142969185
2	182128384	182128385	T	C	22	GENIC	homozygous	136403104
2	182128515	182128516	T	C	24	GENIC	homozygous	136403105