chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	61108854	61108855	T	A	11	GENIC	homozygous	110370645
18	61109614	61109615	C	T	19	GENIC	homozygous	110370647
18	61110784	61110785	A	T	21	GENIC	homozygous	110815337
18	61114852	61114853	G	A	23	GENIC	homozygous	110815341
18	61116660	61116661	T	C	25	GENIC	homozygous	110370655
18	61118108	61118109	A	C	26	GENIC	homozygous	110370659
18	61118257	61118258	C	T	18	GENIC	homozygous	110815343
18	61122138	61122139	T	C	14	GENIC	homozygous	110815347
18	61123263	61123264	A	G	23	GENIC	homozygous	110815349
18	61123792	61123793	A	G	20	GENIC	homozygous	110370663
18	61124275	61124276	C	G	23	GENIC	homozygous	110370665
18	61125191	61125192	G	A	17	GENIC	homozygous	110370669
18	61128129	61128130	T	A	19	GENIC	homozygous	110815351
18	61131309	61131310	T	G	35	GENIC	homozygous	110370675
18	61131415	61131416	C	T	22	GENIC	homozygous	110815353
18	61132251	61132252	C	G	24	GENIC	homozygous	110815355
18	61132255	61132256	C	T	24	GENIC	homozygous	110370677
18	61133751	61133752	C	T	11	GENIC	homozygous	110815357
18	61133937	61133938	A	G	27	GENIC	homozygous	110370679
18	61137146	61137147	T	C	27	GENIC	homozygous	110370685
18	61138640	61138641	A	G	20	GENIC	homozygous	110370691
18	61139809	61139810	C	A	9	GENIC	homozygous	110815359
18	61141630	61141631	T	C	17	GENIC	homozygous	110370693
18	61142164	61142165	C	T	18	GENIC	homozygous	110481051
18	61143190	61143191	C	G	17	GENIC	homozygous	110815361
18	61143563	61143564	G	A	23	GENIC	homozygous	110815363
18	61153189	61153190	A	T	19	GENIC	homozygous	110815365
18	61154153	61154154	A	G	22	GENIC	homozygous	110815367
18	61154264	61154265	G	A	15	GENIC	homozygous	110815369
18	61155198	61155199	T	C	24	GENIC	homozygous	110815371
18	61157043	61157044	A	T	17	GENIC	homozygous	110815373
18	61157335	61157336	G	A	23	GENIC	homozygous	110815375
18	61157994	61157995	T	C	19	GENIC	homozygous	110370707
18	61159380	61159381	A	G	21	GENIC	homozygous	110370709
18	61159637	61159638	G	A	13	GENIC	homozygous	110370711