chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230790527	230790528	A	G	8	GENIC	homozygous	59432908
2	230790540	230790541	A	ATT	6	GENIC	homozygous	60246707
2	230790760	230790761	A	ATT	17	GENIC	homozygous	60246708
2	230791253	230791254	T	TAA	18	GENIC	homozygous	59432910
2	230791872	230791873	A	G	36	GENIC	homozygous	59432911
2	230792047	230792048	T	-	8	GENIC	heterozygous	60520767
2	230792335	230792336	G	GA	16	GENIC	possibly homozygous	60085705
2	230792971	230792972	A	AT	7	GENIC	possibly homozygous	59432914
2	230792971	230792972	A	ATT	7	GENIC	heterozygous	59432915
2	230793374	230793375	C	T	15	GENIC	homozygous	60085707
2	230793686	230793687	G	A	4	GENIC	homozygous	60246710
2	230794074	230794075	G	A	28	GENIC	possibly homozygous	60246711
2	230794101	230794102	G	GA	31	GENIC	homozygous	59432916
2	230794274	230794275	G	A	18	GENIC	homozygous	60246712
2	230794519	230794523	GTGT	----	10	GENIC	heterozygous	60520769
2	230794521	230794523	GT	--	10	GENIC	heterozygous	60896861
2	230794590	230794591	G	-	22	GENIC	homozygous	59432919
2	230795546	230795547	T	C	31	GENIC	homozygous	59432923
2	230796927	230796928	G	T	36	GENIC	homozygous	60246713
2	230797282	230797285	CAC	---	25	GENIC	homozygous	60520770
2	230800972	230800973	T	TTTTC	7	GENIC	homozygous	60085714
2	230792696	230792697	C	G	24	GENIC	homozygous	60419261
2	230793304	230793305	C	T	13	GENIC	homozygous	60419262