chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	115336846	115336846		G	4	GENIC	homozygous	127668036
2	115337443	115337444	A	G	30	GENIC	homozygous	109987359
2	115337455	115337456	G	C	27	GENIC	homozygous	109987361
2	115337657	115337658	A	C	19	GENIC	possibly homozygous	109987363
2	115337921	115337922	G	C	19	GENIC	homozygous	109987364
2	115340324	115340325	G	A	28	GENIC	homozygous	109987366
2	115341312	115341313	G	A	24	GENIC	homozygous	109987368
2	115341587	115341588	C	T	20	GENIC	homozygous	109987370
2	115341633	115341634	G	A	23	GENIC	homozygous	109987372
2	115342624	115342625	C	G	24	GENIC	homozygous	109987374
2	115343356	115343357	A	G	11	GENIC	homozygous	109987376
2	115343371	115343372	A	G	13	GENIC	homozygous	109987377
2	115343716	115343717	T	C	29	GENIC	homozygous	109987379
2	115344071	115344071		CCTG	15	GENIC	homozygous	127668037
2	115344789	115344790	G	A	20	GENIC	homozygous	109987381
2	115345434	115345435	T		22	GENIC	homozygous	127668038
2	115345445	115345446	A	T	23	GENIC	possibly homozygous	109987383
2	115345463	115345464	T	A	21	GENIC	homozygous	109987385
2	115345473	115345474	A	G	23	GENIC	homozygous	109987387
2	115346038	115346039	A	G	30	GENIC	homozygous	109987388
2	115346325	115346326	A	G	32	GENIC	homozygous	109987390
2	115346372	115346372		A	24	GENIC	homozygous	127668039
2	115347724	115347725	A	G	20	GENIC	homozygous	109987392
2	115347892	115347893	T	A	24	GENIC	heterozygous	109987394
2	115348917	115348918	G	T	19	GENIC	homozygous	109987396
2	115349739	115349740	T	G	27	GENIC	homozygous	109987397
2	115352644	115352645	A	G	32	GENIC	homozygous	109987399
2	115351727	115351735	CAATGTAC		29	GENIC	homozygous	127668041