chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	30636361	30636362	G	T	15	GENIC	heterozygous	109675312
2	30637082	30637083	A	T	18	GENIC	homozygous	109675314
2	30642687	30642688	A	T	6	GENIC	homozygous	109675322
2	30642760	30642761	T	C	10	GENIC	homozygous	109675324
2	30642761	30642762	A	G	10	GENIC	homozygous	110501490
2	30645338	30645339	T	G	16	GENIC	homozygous	109675326
2	30646710	30646711	C	T	22	GENIC	homozygous	109675328
2	30646845	30646846	G	A	15	GENIC	homozygous	110501492
2	30648467	30648468	C	A	5	GENIC	heterozygous	110501494
2	30649844	30649845	C	G	4	GENIC	homozygous	109675330
2	30649858	30649859	C	G	6	GENIC	homozygous	109675332
2	30650359	30650360	G	A	20	GENIC	homozygous	109675334
2	30657878	30657879	T	G	18	GENIC	heterozygous	109675338
2	30658401	30658402	A	G	16	GENIC	homozygous	109675340
2	30660382	30660383	T	C	7	GENIC	homozygous	110501504
2	30660722	30660723	C	T	12	GENIC	homozygous	109675344
2	30660727	30660728	A	C	8	GENIC	homozygous	109675346
2	30663707	30663708	A	G	17	GENIC	homozygous	110501508
2	30660381	30660382	G	A	7	GENIC	heterozygous	125717383