chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	207108987	207108988	G	A	24	GENIC	possibly homozygous	59930898
2	207109548	207109549	G	A	6	INTERGENIC	homozygous	59930901
2	207109650	207109651	C	T	14	INTERGENIC	possibly homozygous	60158357
2	207109967	207109968	C	T	15	INTERGENIC	homozygous	60158358
2	207112541	207112542	C	G	23	GENIC	possibly homozygous	59930904
2	207113473	207113474	T	-	2	GENIC	homozygous	59354748
2	207114345	207114346	C	T	30	GENIC	homozygous	59354754
2	207114639	207114640	A	G	29	GENIC	possibly homozygous	59354756
2	207115004	207115005	T	TTTG	3	GENIC	homozygous	59354758
2	207116575	207116576	T	C	12	GENIC	heterozygous	59354769
2	207117080	207117081	G	C	11	GENIC	possibly homozygous	59354774
2	207117212	207117213	T	C	14	GENIC	heterozygous	59354778
2	207117821	207117822	G	T	12	GENIC	heterozygous	60158361
2	207121109	207121110	A	G	13	GENIC	heterozygous	59930910
2	207121145	207121146	A	AG	10	GENIC	homozygous	59354795
2	207121560	207121561	C	T	15	GENIC	homozygous	59930911
2	207121806	207121807	G	A	13	GENIC	possibly homozygous	59354797
2	207124836	207124837	G	T	1	GENIC	homozygous	59354806
2	207125638	207125639	C	G	20	GENIC	homozygous	59354810
2	207126232	207126233	T	C	29	GENIC	homozygous	59930916
2	207126495	207126496	T	C	24	GENIC	homozygous	59354813
2	207127238	207127239	G	T	21	GENIC	homozygous	60158365
2	207127920	207127921	A	G	10	GENIC	homozygous	59354816