chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	50382953	50382954	G		29	GENIC	homozygous	138888433
11	50394027	50394028	C	T	31	GENIC	homozygous	138989810
11	50394034	50394040	CCACAC		27	GENIC	homozygous	138888438
11	50394049	50394050	C	T	18	GENIC	heterozygous	403305753
11	50394045	50394046	C	T	18	GENIC	heterozygous	403305751
11	50394045	50394046	C		18	GENIC	heterozygous	403305750
11	50394049	50394050	C		18	GENIC	heterozygous	403305752
11	50394055	50394056	C		18	GENIC	heterozygous	403305754
11	50394055	50394056	C	T	18	GENIC	heterozygous	403305755
11	50394110	50394111	A	T	36	GENIC	homozygous	138989811
11	50408291	50408292	G		14	GENIC	heterozygous	403305762
11	50408291	50408292	G	C	14	GENIC	heterozygous	403305763
11	50408293	50408294	G		14	GENIC	heterozygous	403305764
11	50408293	50408294	G	C	14	GENIC	heterozygous	403305765
11	50408295	50408296	G		14	GENIC	heterozygous	403305766
11	50408295	50408296	G	C	14	GENIC	heterozygous	403305767
11	50444259	50444260	A		12	GENIC	heterozygous	403305775
11	50444259	50444260	A	G	12	GENIC	heterozygous	403305776
11	50479286	50479287	T	A	29	GENIC	possibly homozygous	141038748
11	50479288	50479289	T	A	31	GENIC	heterozygous	138989868
11	50479288	50479289	T		31	GENIC	heterozygous	403305781
11	50481180	50481181	C		21	GENIC	heterozygous	403305782
11	50481180	50481181	C	T	21	GENIC	heterozygous	403305783
11	50517852	50517853	G	A	6	GENIC	homozygous	138989894
11	50479282	50479283	T	A	29	GENIC	possibly homozygous	403641066
11	50479282	50479283	T		29	GENIC	heterozygous	403641067
11	50479286	50479287	T		29	GENIC	heterozygous	403641068
11	50621427	50621428	T		19	GENIC	heterozygous	403305797
11	50621427	50621428	T	C	19	GENIC	heterozygous	403305798
11	50623923	50623924	C		16	GENIC	homozygous	403305801
11	50623923	50623924	C	A	16	GENIC	heterozygous	403305802