chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31561169	31561170	T	C	32	GENIC	homozygous	115811940
11	31562281	31562282	C	A	11	GENIC	homozygous	115811944
11	31563345	31563346	C	T	25	GENIC	homozygous	115811948
11	31564585	31564586	T	G	26	GENIC	homozygous	116096717
11	31564637	31564638	G	C	29	GENIC	homozygous	116096719
11	31564841	31564842	G	C	29	GENIC	homozygous	115811950
11	31564843	31564844	A	G	30	GENIC	homozygous	115811952
11	31564855	31564856	T	A	31	GENIC	homozygous	115811954
11	31565518	31565519	G	A	33	GENIC	homozygous	115811958
11	31565519	31565520	A	G	34	GENIC	homozygous	115811960
11	31565725	31565726	C	A	51	GENIC	homozygous	115811962
11	31565992	31565993	C	T	19	GENIC	homozygous	116035365
11	31566388	31566389	T	G	25	GENIC	homozygous	115811968
11	31566474	31566475	T	C	25	GENIC	homozygous	115811970
11	31568362	31568363	C	T	41	GENIC	homozygous	115811972
11	31569300	31569301	A	G	27	GENIC	homozygous	115811974
11	31571741	31571742	T	C	25	GENIC	homozygous	115811978
11	31572685	31572686	G	A	35	GENIC	homozygous	115811980
11	31576014	31576015	C	A	23	GENIC	possibly homozygous	115811984
11	31576560	31576561	C	T	24	GENIC	homozygous	115811986
11	31577721	31577722	G	A	40	GENIC	homozygous	115811988
11	31578086	31578087	A	T	21	GENIC	homozygous	115811990
11	31578099	31578100	T	A	23	GENIC	homozygous	115811992
11	31578100	31578101	A	G	23	GENIC	homozygous	115811994
11	31578137	31578138	C	T	23	GENIC	homozygous	115811996
11	31581178	31581179	A	G	33	GENIC	possibly homozygous	115811998
11	31581398	31581399	T	C	31	GENIC	possibly homozygous	115812000
11	31581763	31581764	G	A	32	GENIC	possibly homozygous	115812002
11	31582272	31582273	T	C	18	GENIC	homozygous	115812004
11	31582340	31582341	T	G	15	GENIC	homozygous	115812006
11	31580909	31580910	T	C	28	GENIC	homozygous	115960345