chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	1381745	1381746	T	G	10	GENIC	homozygous	60660157
2	1383092	1383093	C	G	13	GENIC	homozygous	62042477
2	1385325	1385326	T	C	15	GENIC	homozygous	60660162
2	1389519	1389520	T	TG	12	GENIC	homozygous	62042478
2	1389520	1389521	T	C	12	GENIC	homozygous	62042479
2	1390788	1390789	T	A	22	GENIC	homozygous	62042480
2	1390849	1390850	A	G	27	GENIC	homozygous	62042481
2	1393869	1393870	G	A	13	GENIC	homozygous	60660185
2	1397298	1397299	A	ATTT	8	GENIC	homozygous	62448392
2	1397472	1397473	T	C	12	GENIC	homozygous	60660190
2	1399871	1399872	G	A	14	GENIC	homozygous	60660192
2	1400189	1400190	G	A	16	GENIC	homozygous	60660195
2	1412967	1412968	T	A	15	GENIC	homozygous	60952053
2	1415796	1415797	T	-	13	GENIC	homozygous	60952057
2	1415800	1415801	C	G	13	GENIC	homozygous	60952060
2	1417093	1417094	T	C	27	GENIC	homozygous	60660200
2	1417715	1417716	C	A	13	GENIC	homozygous	60660202
2	1417718	1417719	C	A	16	GENIC	homozygous	60660205
2	1418201	1418202	C	T	19	GENIC	homozygous	60660208