chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	237334877	237334878	T	-	16	GENIC	homozygous	59946473
2	237334979	237334980	G	A	15	GENIC	homozygous	59946474
2	237335141	237335142	C	T	6	GENIC	homozygous	59946475
2	237335359	237335360	T	C	17	GENIC	homozygous	59455352
2	237335793	237335794	A	C	12	GENIC	homozygous	59946477
2	237335971	237335972	C	T	17	GENIC	homozygous	59946478
2	237336068	237336069	A	AATAT	6	GENIC	homozygous	59946479
2	237336646	237336647	T	-	7	GENIC	homozygous	59776841
2	237337022	237337023	T	C	22	GENIC	possibly homozygous	59946480
2	237337297	237337298	A	G	20	GENIC	homozygous	59946481
2	237337563	237337564	A	G	15	GENIC	homozygous	59455357
2	237338873	237338874	A	AACACACACACACAC	6	GENIC	heterozygous	60562315
2	237338873	237338874	A	AACACACACACAC	6	GENIC	heterozygous	60551396
2	237339277	237339278	C	G	27	GENIC	homozygous	59946482
2	237339338	237339339	A	-	12	GENIC	homozygous	59946483
2	237339343	237339347	GGCG	----	12	GENIC	homozygous	59776843
2	237339583	237339584	G	A	8	GENIC	homozygous	59946484
2	237339596	237339597	T	TTCTCTCTCTC	4	GENIC	homozygous	60522148
2	237339742	237339743	C	CT	19	GENIC	possibly homozygous	59946485
2	237340315	237340316	A	G	20	GENIC	homozygous	59946486