chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31807509	31807510	T	G	46	GENIC	homozygous	115812546
11	31809830	31809831	A	C	32	GENIC	homozygous	115812548
11	31810848	31810849	G	A	39	GENIC	homozygous	115812550
11	31811323	31811324	T	G	41	GENIC	homozygous	115812552
11	31812086	31812087	T	G	37	GENIC	homozygous	115812554
11	31814136	31814137	C	A	40	GENIC	possibly homozygous	115812556
11	31816607	31816608	C	T	37	GENIC	possibly homozygous	115812558
11	31816630	31816631	T	C	37	GENIC	homozygous	115812560
11	31817271	31817272	G	A	48	GENIC	homozygous	115812562
11	31819506	31819507	C	T	45	GENIC	homozygous	115812564
11	31819718	31819719	C	A	54	GENIC	homozygous	115812566
11	31819852	31819853	C	G	55	GENIC	homozygous	115812568
11	31824599	31824600	A	C	49	GENIC	homozygous	115812570
11	31826107	31826108	T	C	55	GENIC	homozygous	115812572
11	31826193	31826194	T	C	34	GENIC	homozygous	115812574
11	31826694	31826695	A	T	39	GENIC	homozygous	115812576
11	31827086	31827087	T	C	42	GENIC	homozygous	115812578
11	31828242	31828243	G	A	32	GENIC	homozygous	115812580
11	31828669	31828670	C	G	41	GENIC	homozygous	115812582
11	31829541	31829542	G	A	40	GENIC	homozygous	115812584
11	31833603	31833604	T	C	43	GENIC	homozygous	115812586
11	31834188	31834189	T	C	38	GENIC	possibly homozygous	116416052
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