chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	234200131	234200132	C	T	7	GENIC	homozygous	127839390
2	234200232	234200233	T	C	9	GENIC	homozygous	110837954
2	234200737	234200738	C	T	7	GENIC	homozygous	127839391
2	234200767	234200768	A	G	11	GENIC	homozygous	131322514
2	234207528	234207529	T	C	2	GENIC	homozygous	110912818
2	234207574	234207575	G	A	2	GENIC	homozygous	120298740
2	234207577	234207583	CGCGCA		2	GENIC	homozygous	131303069
2	234213825	234213826	G	C	4	GENIC	homozygous	127839392
2	234213929	234213933	TTTG		12	GENIC	homozygous	127749626
2	234214742	234214743	T	C	18	GENIC	homozygous	127839393
2	234224838	234224839	T	A	4	GENIC	homozygous	110837956
2	234247032	234247033	A	G	4	GENIC	homozygous	110311503
2	234247115	234247116	T	G	6	GENIC	homozygous	132579651
2	234247117	234247122	TTTTT		6	GENIC	homozygous	127749628
2	234247188	234247189	A	G	2	GENIC	homozygous	110837958
2	234247619	234247620	G	A	4	GENIC	homozygous	127839397
2	234255893	234255894	C	A	2	GENIC	homozygous	134123412
2	234274385	234274386	T	C	4	GENIC	homozygous	127839399
2	234274726	234274727	A	G	23	GENIC	homozygous	110311505
2	234274928	234274929	G	A	11	GENIC	homozygous	110311507
2	234274966	234274967	C	A	4	GENIC	homozygous	110311509
2	234275303	234275304	G	A	9	GENIC	homozygous	127839400