chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	200487055	200487056	C	A	14	GENIC	homozygous	111000366
2	200492803	200492804	A	G	12	GENIC	homozygous	110204618
2	200493865	200493866	T	C	18	GENIC	possibly homozygous	110204632
2	200493867	200493867		CA	17	GENIC	possibly homozygous	131299668
2	200497048	200497049	T	C	11	GENIC	homozygous	110204664
2	200498717	200498718	G	A	16	GENIC	homozygous	111000370
2	200499992	200499993	A	G	23	GENIC	homozygous	111000372
2	200501332	200501333	T	A	16	GENIC	homozygous	111000374
2	200501335	200501336	G	A	15	GENIC	homozygous	111000376
2	200501348	200501349	T	G	19	GENIC	homozygous	111000378
2	200501570	200501571	G	A	28	GENIC	possibly homozygous	111000380
2	200501605	200501606	T	G	25	GENIC	possibly homozygous	133719850
2	200501665	200501666	A	G	22	GENIC	homozygous	127833941
2	200507955	200507956	A	T	23	GENIC	homozygous	111000382
2	200508890	200508891	T	C	20	GENIC	homozygous	111000384
2	200510138	200510139	T	C	23	GENIC	homozygous	110204725
2	200510706	200510707	C	T	22	GENIC	homozygous	111000390
2	200512085	200512086	C	G	24	GENIC	homozygous	111000392
2	200512774	200512775	T	C	15	GENIC	homozygous	110204730