chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	237659800	237659801	G	C	32	GENIC	homozygous	59946841
2	237660590	237660591	C	T	30	GENIC	possibly homozygous	59946842
2	237661476	237661477	G	-	15	GENIC	heterozygous	59946843
2	237661981	237661982	A	-	9	GENIC	homozygous	59946844
2	237662017	237662018	G	A	11	GENIC	heterozygous	59946846
2	237663064	237663065	T	-	39	GENIC	homozygous	59946848
2	237663286	237663287	T	G	26	GENIC	homozygous	59946849
2	237663445	237663446	T	C	21	GENIC	homozygous	59946850
2	237663581	237663582	T	G	19	GENIC	homozygous	59946851
2	237663719	237663720	C	-	26	GENIC	homozygous	59946852
2	237663798	237663799	A	G	22	GENIC	homozygous	59946853
2	237664342	237664343	T	-	21	GENIC	homozygous	59946854
2	237664348	237664349	T	A	21	GENIC	homozygous	59946856
2	237664386	237664387	C	T	30	GENIC	homozygous	59946857
2	237664670	237664671	T	C	36	GENIC	homozygous	59946858
2	237664899	237664900	G	A	27	GENIC	possibly homozygous	59946859
2	237665056	237665057	A	T	29	GENIC	homozygous	59946860
2	237665232	237665233	G	A	26	GENIC	possibly homozygous	59946861
2	237662404	237662405	T	TTGTGTGTG	10	GENIC	homozygous	60522226
2	237663070	237663071	T	A	40	GENIC	homozygous	60459612
2	237666097	237666098	G	A	36	GENIC	homozygous	59455804
2	237667966	237667967	T	C	35	GENIC	homozygous	59946862
2	237669551	237669552	T	-	4	GENIC	homozygous	60595893
2	237671042	237671043	G	A	24	GENIC	homozygous	59946865
2	237673600	237673604	GTGT	----	6	GENIC	homozygous	60595895
2	237677868	237677869	C	G	25	GENIC	homozygous	59946868
2	237678376	237678377	G	A	24	GENIC	homozygous	59946869
2	237679183	237679184	T	C	17	GENIC	possibly homozygous	59946870
2	237679382	237679383	A	G	33	GENIC	homozygous	59946871
2	237679538	237679539	A	T	33	GENIC	homozygous	59946872
2	237679752	237679753	A	G	21	GENIC	homozygous	59455810
2	237679839	237679840	T	C	36	GENIC	homozygous	59946873
2	237679991	237679992	T	C	34	GENIC	homozygous	59946874
2	237673770	237673771	C	CA	1	GENIC	homozygous	60551472