chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	30636361	30636362	G	T	14	GENIC	homozygous	109675312
2	30637082	30637083	A	T	30	GENIC	homozygous	109675314
2	30642687	30642688	A	T	16	GENIC	homozygous	109675322
2	30642760	30642761	T	C	13	GENIC	homozygous	109675324
2	30642761	30642762	A	G	13	GENIC	homozygous	110501490
2	30645338	30645339	T	G	23	GENIC	homozygous	109675326
2	30646710	30646711	C	T	13	GENIC	homozygous	109675328
2	30646845	30646846	G	A	16	GENIC	homozygous	110501492
2	30649858	30649859	C	G	16	GENIC	homozygous	109675332
2	30650359	30650360	G	A	24	GENIC	homozygous	109675334
2	30656925	30656926	T	C	31	GENIC	heterozygous	110885746
2	30657878	30657879	T	G	23	GENIC	homozygous	109675338
2	30658401	30658402	A	G	21	GENIC	homozygous	109675340
2	30659977	30659978	A	G	27	GENIC	homozygous	109675342
2	30660722	30660723	C	T	14	GENIC	homozygous	109675344
2	30660727	30660728	A	C	17	GENIC	homozygous	109675346
2	30663707	30663708	A	G	20	GENIC	homozygous	110501508
2	30664172	30664173	C	G	38	GENIC	homozygous	110501510
2	30664247	30664248	G	A	22	GENIC	homozygous	109675348
2	30657106	30657107	A	G	38	GENIC	heterozygous	110678292
2	30656917	30656918	T	C	30	GENIC	heterozygous	111098455
2	30656997	30656998	C	T	30	GENIC	heterozygous	110678290