chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	1381745	1381746	T	G	8	GENIC	homozygous	60660157
2	1383880	1383881	A	G	7	GENIC	homozygous	60660159
2	1385325	1385326	T	C	11	GENIC	possibly homozygous	60660162
2	1389520	1389521	T	G	11	GENIC	homozygous	60660165
2	1389531	1389532	A	G	11	GENIC	homozygous	60660167
2	1389594	1389595	A	G	15	GENIC	homozygous	60660172
2	1389611	1389612	T	C	12	GENIC	possibly homozygous	60660175
2	1389994	1389995	C	T	16	GENIC	homozygous	60660177
2	1393869	1393870	G	A	14	GENIC	possibly homozygous	60660185
2	1394213	1394214	C	T	15	GENIC	homozygous	60660187
2	1397472	1397473	T	C	19	GENIC	homozygous	60660190
2	1399871	1399872	G	A	17	GENIC	homozygous	60660192
2	1400189	1400190	G	A	9	GENIC	possibly homozygous	60660195
2	1397298	1397299	A	ATT	1	GENIC	homozygous	62142467
2	1407669	1407670	A	-	7	GENIC	homozygous	62142470
2	1409032	1409033	C	T	11	GENIC	homozygous	62142473
2	1413699	1413703	CCTA	----	5	GENIC	homozygous	60660197
2	1417093	1417094	T	C	19	GENIC	homozygous	60660200
2	1417715	1417716	C	A	1	GENIC	homozygous	60660202
2	1417718	1417719	C	A	5	GENIC	homozygous	60660205
2	1418201	1418202	C	T	23	GENIC	possibly homozygous	60660208
2	1419590	1419591	A	G	11	GENIC	homozygous	62142484