chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	234200131	234200132	C	T	10	GENIC	homozygous	127839390
2	234200232	234200233	T	C	7	GENIC	homozygous	110837954
2	234200737	234200738	C	T	6	GENIC	homozygous	127839391
2	234213825	234213826	G	C	9	GENIC	homozygous	127839392
2	234214742	234214743	T	C	9	GENIC	homozygous	127839393
2	234224838	234224839	T	A	5	GENIC	homozygous	110837956
2	234247032	234247033	A	G	2	GENIC	homozygous	110311503
2	234200767	234200768	A	G	5	GENIC	homozygous	131322514
2	234207528	234207529	T	C	1	GENIC	homozygous	110912818
2	234207574	234207575	G	A	3	GENIC	homozygous	120298740
2	234207617	234207617		A	2	GENIC	homozygous	131606310
2	234247115	234247116	T	G	3	GENIC	homozygous	132579651
2	234256453	234256454	T		5	GENIC	homozygous	130255479
2	234213929	234213933	TTTG		8	GENIC	homozygous	127749626
2	234247117	234247122	TTTTT		3	GENIC	homozygous	127749628
2	234207577	234207583	CGCGCA		3	GENIC	homozygous	131303069
2	234256443	234256443		G	5	GENIC	homozygous	130255477
2	234256447	234256447		G	5	GENIC	homozygous	130255478
2	234256458	234256458		A	5	GENIC	homozygous	130255480
2	234274385	234274386	T	C	4	GENIC	homozygous	127839399
2	234274726	234274727	A	G	10	GENIC	homozygous	110311505
2	234275303	234275304	G	A	5	GENIC	homozygous	127839400