chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31566388	31566389	T	G	16	GENIC	homozygous	115811968
11	31566474	31566475	T	C	16	GENIC	homozygous	115811970
11	31568362	31568363	C	T	9	GENIC	homozygous	115811972
11	31569300	31569301	A	G	9	GENIC	homozygous	115811974
11	31571741	31571742	T	C	20	GENIC	homozygous	115811978
11	31572685	31572686	G	A	13	GENIC	homozygous	115811980
11	31576014	31576015	C	A	20	GENIC	homozygous	115811984
11	31576560	31576561	C	T	14	GENIC	homozygous	115811986
11	31577721	31577722	G	A	24	GENIC	homozygous	115811988
11	31578086	31578087	A	T	10	GENIC	homozygous	115811990
11	31578099	31578100	T	A	4	GENIC	heterozygous	115811992
11	31578100	31578101	A	G	4	GENIC	homozygous	115811994
11	31578137	31578138	C	T	13	GENIC	homozygous	115811996
11	31581178	31581179	A	G	18	GENIC	homozygous	115811998
11	31581398	31581399	T	C	23	GENIC	homozygous	115812000
11	31581763	31581764	G	A	13	GENIC	homozygous	115812002
11	31582272	31582273	T	C	16	GENIC	homozygous	115812004
11	31582340	31582341	T	G	24	GENIC	homozygous	115812006
11	31580909	31580910	T	C	22	GENIC	homozygous	115960345