chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31834871	31834872	T	C	57	GENIC	homozygous	115812588
11	31835709	31835710	T	C	38	GENIC	homozygous	115812590
11	31836290	31836291	C	T	50	GENIC	homozygous	115812592
11	31836441	31836442	G	A	40	GENIC	homozygous	115812594
11	31836478	31836479	A	T	38	GENIC	homozygous	115812596
11	31839222	31839223	C	T	59	GENIC	homozygous	115812598
11	31839512	31839513	G	A	57	GENIC	homozygous	115812600
11	31839878	31839879	T	G	53	GENIC	homozygous	115812602
11	31840390	31840391	G	T	38	GENIC	homozygous	115812604
11	31840391	31840392	A	T	38	GENIC	possibly homozygous	115812606
11	31842127	31842128	A	C	33	GENIC	homozygous	115812608
11	31842129	31842130	A	G	35	GENIC	homozygous	115812610
11	31842717	31842718	C	T	49	GENIC	homozygous	115812612
11	31844268	31844269	C	A	45	GENIC	heterozygous	118141606
11	31845576	31845577	C	T	42	GENIC	homozygous	115812614
11	31845812	31845813	T	A	57	GENIC	homozygous	115812616
11	31846621	31846622	T	C	51	GENIC	homozygous	115812618
11	31846831	31846832	C	T	38	GENIC	homozygous	115812620
11	31847704	31847705	A	G	44	GENIC	homozygous	115812622
11	31838809	31838810	C	T	40	GENIC	homozygous	115960366
11	31841601	31841602	A	T	45	GENIC	possibly homozygous	115960367
11	31844805	31844806	G	A	52	GENIC	homozygous	115960368