chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	115337443	115337444	A	G	7	GENIC	homozygous	109987359
2	115337455	115337456	G	C	7	GENIC	homozygous	109987361
2	115337921	115337922	G	C	18	GENIC	homozygous	109987364
2	115339787	115339788	G	A	22	GENIC	homozygous	120205105
2	115341633	115341634	G	A	18	GENIC	homozygous	109987372
2	115342516	115342517	A	T	20	GENIC	homozygous	120205106
2	115342624	115342625	C	G	22	GENIC	homozygous	109987374
2	115343371	115343372	A	G	12	GENIC	homozygous	109987377
2	115343716	115343717	T	C	19	GENIC	homozygous	109987379
2	115343927	115343928	G	A	23	GENIC	homozygous	120205107
2	115344066	115344067	T	C	13	GENIC	homozygous	120205108
2	115344071	115344071		CCTG	12	GENIC	homozygous	127668037
2	115345463	115345464	T	A	25	GENIC	homozygous	109987385
2	115346325	115346326	A	G	18	GENIC	homozygous	109987390
2	115346372	115346372		A	22	GENIC	homozygous	127668039
2	115347724	115347725	A	G	9	GENIC	homozygous	109987392
2	115348436	115348448	CCTGCTGCTCCC		2	GENIC	homozygous	127668040
2	115349739	115349740	T	G	19	GENIC	homozygous	109987397
2	115349992	115349993	T	C	23	GENIC	homozygous	120205109
2	115351008	115351009	T	G	20	GENIC	homozygous	120205110
2	115351656	115351657	C	A	23	GENIC	homozygous	120205111
2	115352644	115352645	A	G	18	GENIC	homozygous	109987399